A Study to Assess the Effectiveness and Safety of Rivaroxaban in Reducing the Risk of Death, Myocardial Infarction or Stroke in Participants With Heart Failure and Coronary Artery Disease Following an Episode of Decompensated Heart Failure

NCT ID: NCT01877915

Last Updated: 2019-05-10

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

5081 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-09-10

Study Completion Date

2018-04-19

Brief Summary

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The purpose of this study is to assess the effectiveness and safety of rivaroxaban compared with placebo (inactive medication), in reducing the risk of death, myocardial infarction or stroke in participants with heart failure and significant coronary artery disease following an episode of decompensated heart failure.

Detailed Description

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This is a randomized (the study medication is assigned by chance), double-blind (neither physician nor participant knows the identity of the assigned treatment), parallel group (each participant group receives different treatments simultaneously), event driven (the study duration is determined by the time taken for a specific number of events to occur), multicenter study to assess the effectiveness and safety of rivaroxaban compared with placebo, in reducing the risk of death, myocardial infarction or stroke in participants with heart failure and significant coronary artery disease following an episode of decompensated heart failure. Participants will be randomly assigned in a 1:1 ratio to receive either rivaroxaban or placebo (each in addition to standard of care for heart failure and coronary artery disease as prescribed by their managing physician). The study will consist of a screening phase, a double-blind treatment phase, and a follow-up after the sponsor-announced global treatment end date (GTED, defined as the date when 1200 primary efficacy outcome events are predicted to have occurred). The double-blind treatment phase is estimated to last for 6 to 54 months. Participants will discontinue study drug after taking both their morning and evening doses on the GTED and will return to the study center for the end-of-study visit (between 15 and 45 days but no sooner than 15 days after the GTED). Patient safety will be monitored throughout the study. The average study duration for participants is expected to be approximately 29 months. The study drug, rivaroxaban, is approved in the United States and in multiple countries around the world for the prevention and treatment of a number of thrombosis-mediated conditions.

Conditions

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Heart Failure Coronary Artery Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Rivaroxaban 2.5 mg

Each participant will receive 2.5 mg of rivaroxaban twice daily with standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician).

Group Type EXPERIMENTAL

Rivaroxaban

Intervention Type DRUG

Each participant, randomly allocated to the rivaroxaban arm, will receive one 2.5 mg tablet of rivaroxaban orally (by mouth) twice daily (once in the morning and once in the evening at approximately the same time each day) until the global treatment end date (GTED) (defined as the date when 1200 primary efficacy outcome events have occurred). Rivaroxaban will be given with standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician).

Standard of care for heart failure and coronary artery disease

Intervention Type OTHER

Each participant's standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician) should be continued throughout the study.

Placebo

Each participant will receive matching placebo twice daily with standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician).

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Each participant, randomly allocated to the placebo arm, will receive one matching placebo tablet orally twice daily (once in the morning and once in the evening at approximately the same time each day) until the GTED. Placebo will be given with standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician).

Standard of care for heart failure and coronary artery disease

Intervention Type OTHER

Each participant's standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician) should be continued throughout the study.

Interventions

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Rivaroxaban

Each participant, randomly allocated to the rivaroxaban arm, will receive one 2.5 mg tablet of rivaroxaban orally (by mouth) twice daily (once in the morning and once in the evening at approximately the same time each day) until the global treatment end date (GTED) (defined as the date when 1200 primary efficacy outcome events have occurred). Rivaroxaban will be given with standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician).

Intervention Type DRUG

Placebo

Each participant, randomly allocated to the placebo arm, will receive one matching placebo tablet orally twice daily (once in the morning and once in the evening at approximately the same time each day) until the GTED. Placebo will be given with standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician).

Intervention Type DRUG

Standard of care for heart failure and coronary artery disease

Each participant's standard of care for heart failure and coronary artery disease (as prescribed by the participant's managing physician) should be continued throughout the study.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Must have symptomatic heart failure for at least 3 months prior to Screening
* Participants must have an episode of decompensated heart failure (index event) requiring (a) an overnight stay \[that is, staying past midnight\] in a hospital, emergency department, or medical facility with the capability of treating with intravenous medications and observing heart failure patients before randomization or (b) an unscheduled outpatient visit to a heart failure management center, where parenteral therapy is required for heart failure stabilization. An episode of decompensated heart failure is defined as symptoms of worsening dyspnea or fatigue, objective signs of congestion such as peripheral edema or ascites, and/or adjustment of pre-hospitalization/outpatient visit heart failure medications. Participants are eligible for randomization at discharge from the facility treating the index event and up to 30 days after discharge if they are in stable condition
* Must have a documented left ventricular ejection fraction (LVEF) of less than or equal to 40 percent (%) within 1 year before randomization
* Must have evidence of significant coronary artery disease
* Must be medically stable in terms of their heart failure clinical status at the time of randomization
* Must have a brain natriuretic peptide (BNP) level greater than or equal to (\>=) 200 picogram per milliliter (pg/mL) or N-terminal-proBNP (NT-proBNP) level \>=800 pg/mL (preferred assay) during the Screening period and before randomization

Exclusion Criteria

* Any condition that, in the opinion of the investigator, contraindicates anticoagulant therapy or would have an unacceptable risk of bleeding, such as, but not limited to, active internal bleeding, clinically significant bleeding, bleeding at a noncompressible site, or bleeding diathesis within 28 days of randomization
* Severe concomitant disease such as (a) atrial fibrillation (AFib) or another condition that requires chronic anticoagulation (participants with isolated transient AFib may be allowed at the discretion of the treating physician investigator) and (b) Documented acute myocardial infarction (MI) during index event
* Prior stroke within 90 days of randomization
* Has been hospitalized for longer than 21 days during the index event
* Planned intermittent outpatient treatment with positive inotropic drugs administered intravenously
Minimum Eligible Age

18 Years

Maximum Eligible Age

95 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bayer

INDUSTRY

Sponsor Role collaborator

Janssen Research & Development, LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Janssen Research & Development, LLC Clinical Trial

Role: STUDY_DIRECTOR

Janssen Research & Development, LLC

Locations

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Kuala Lumpur, , Malaysia

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Kuala Selangor, , Malaysia

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Kuching, , Malaysia

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Selayang Baru Utara, , Malaysia

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Aguascalientes, , Mexico

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Benito Juárez, , Mexico

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Chihuahua City, , Mexico

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Alexander City, Alabama, United States

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Birmingham, Alabama, United States

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Mobile, Alabama, United States

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Anchorage, Alaska, United States

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Tucson, Arizona, United States

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Jonesboro, Arkansas, United States

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Beverly Hills, California, United States

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Chula Vista, California, United States

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El Cajon, California, United States

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Glendale, California, United States

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La Mesa, California, United States

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Los Angeles, California, United States

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Newport Beach, California, United States

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Orange, California, United States

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Stockton, California, United States

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Torrance, California, United States

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Aurora, Colorado, United States

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Denver, Colorado, United States

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New Haven, Connecticut, United States

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Atlantis, Florida, United States

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Daytona Beach, Florida, United States

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Jupiter, Florida, United States

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Orlando, Florida, United States

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St. Petersburg, Florida, United States

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Tallahassee, Florida, United States

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Wellington, Florida, United States

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Winter Haven, Florida, United States

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Athens, Georgia, United States

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Atlanta, Georgia, United States

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Cumming, Georgia, United States

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Macon, Georgia, United States

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Tucker, Georgia, United States

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Chicago, Illinois, United States

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Evanston, Illinois, United States

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Fairview Heights, Illinois, United States

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Peoria, Illinois, United States

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Rockford, Illinois, United States

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Urbana, Illinois, United States

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Anderson, Indiana, United States

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Indianapolis, Indiana, United States

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Merrillville, Indiana, United States

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Munster, Indiana, United States

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South Bend, Indiana, United States

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Iowa City, Iowa, United States

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Elizabethtown, Kentucky, United States

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Lexington, Kentucky, United States

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Louisville, Kentucky, United States

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Owensboro, Kentucky, United States

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Bossier City, Louisiana, United States

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Hammond, Louisiana, United States

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Shreveport, Louisiana, United States

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Slidell, Louisiana, United States

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Biddeford, Maine, United States

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Baltimore, Maryland, United States

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Columbia, Maryland, United States

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Randallstown, Maryland, United States

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Bay City, Michigan, United States

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Grand Blanc, Michigan, United States

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Mount Clemens, Michigan, United States

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Pontiac, Michigan, United States

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Ypsilanti, Michigan, United States

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Saint Paul, Minnesota, United States

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Springfield, Missouri, United States

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St Louis, Missouri, United States

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Washington, Missouri, United States

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Lincoln, Nebraska, United States

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Las Vegas, Nevada, United States

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Bridgewater, New Jersey, United States

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Elmer, New Jersey, United States

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Haddon Heights, New Jersey, United States

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Manalapan, New Jersey, United States

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Ridgewood, New Jersey, United States

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Sewell, New Jersey, United States

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Albuquerque, New Mexico, United States

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Buffalo, New York, United States

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Cortlandt Manor, New York, United States

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Jamaica, New York, United States

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Mineola, New York, United States

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New York, New York, United States

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Charlotte, North Carolina, United States

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High Point, North Carolina, United States

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Pinehurst, North Carolina, United States

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Canton, Ohio, United States

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Cincinnati, Ohio, United States

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Columbus, Ohio, United States

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Dayton, Ohio, United States

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Fairfield, Ohio, United States

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Kettering, Ohio, United States

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Bartlesville, Oklahoma, United States

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Oklahoma City, Oklahoma, United States

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Tulsa, Oklahoma, United States

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Portland, Oregon, United States

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Doylestown, Pennsylvania, United States

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Philadelphia, Pennsylvania, United States

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Sayre, Pennsylvania, United States

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Sellersville, Pennsylvania, United States

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Wynnewood, Pennsylvania, United States

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Yardley, Pennsylvania, United States

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York, Pennsylvania, United States

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Charleston, South Carolina, United States

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Sioux Falls, South Dakota, United States

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Nashville, Tennessee, United States

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Cypress, Texas, United States

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Dallas, Texas, United States

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Fort Worth, Texas, United States

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Houston, Texas, United States

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Huntsville, Texas, United States

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Kingwood, Texas, United States

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Lubbock, Texas, United States

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McKinney, Texas, United States

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Burlington, Vermont, United States

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Newport News, Virginia, United States

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Bellingham, Washington, United States

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Tacoma, Washington, United States

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Huntington, West Virginia, United States

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Bahía Blanca, , Argentina

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Buenos Aires, , Argentina

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Caba, , Argentina

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Córdoba, , Argentina

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La Plata, , Argentina

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Mar del Plata, , Argentina

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Mendoza, , Argentina

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Merlo, , Argentina

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Quilmes, , Argentina

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Resistencia, , Argentina

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Rosario, , Argentina

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San Miguel de Tucumán, , Argentina

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San Nicolás, , Argentina

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Santa Fe, , Argentina

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Santiago del Estero, , Argentina

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Vicente López, , Argentina

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Bedford, , Australia

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Cairns, , Australia

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Concord, , Australia

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Darlinghurst, , Australia

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Hobart, , Australia

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Launceston, , Australia

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Perth, , Australia

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Sydney, , Australia

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Wollongong, , Australia

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Woolloongabba, , Australia

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Belém, , Brazil

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Belo Horizonte, , Brazil

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Blumenal, , Brazil

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Brasília, , Brazil

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Campina Grande do Sul, , Brazil

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Campinas, , Brazil

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Campo Grande, , Brazil

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Canoas, , Brazil

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Curitiba, , Brazil

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Goiânia, , Brazil

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Marília, , Brazil

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Passo Fundo, , Brazil

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Porto Alegre, , Brazil

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Recife, , Brazil

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Ribeirão Preto, , Brazil

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Rio de Janeiro, , Brazil

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Salvador, , Brazil

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São Jose Do Rio Preto, , Brazil

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São Paulo, , Brazil

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São Pedro, , Brazil

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Tatuí, , Brazil

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Uberlândia, , Brazil

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Votuporanga, , Brazil

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Blagoevgrad, , Bulgaria

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Burgas, , Bulgaria

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Dimitrovgrad, , Bulgaria

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Kazanlak, , Bulgaria

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Pazardzhik, , Bulgaria

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Pleven, , Bulgaria

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Plovdiv, , Bulgaria

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Rousse, , Bulgaria

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Sofia, , Bulgaria

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Stara Zagora, , Bulgaria

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Varna, , Bulgaria

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Veliko Tarnovo, , Bulgaria

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Edmonton, Alberta, Canada

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Maple Ridge, British Columbia, Canada

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St. John's, Newfoundland and Labrador, Canada

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Halifax, Nova Scotia, Canada

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Cambridge, Ontario, Canada

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Kitchener, Ontario, Canada

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London, Ontario, Canada

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Ottawa, Ontario, Canada

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Scarborough Village, Ontario, Canada

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Toronto, Ontario, Canada

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Montreal, Quebec, Canada

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Baotou, , China

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Beijing, , China

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Changchun, , China

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Changsha, , China

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Chengdu, , China

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Daqing, , China

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Guangzhou, , China

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Haikou, , China

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Hangzhou, , China

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Hunan, , China

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Jinan, , China

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Jining, , China

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Lanzhou, , China

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Nanchang, , China

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Nanjing, , China

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Nanning, , China

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Qingdao, , China

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Shanghai, , China

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Shenyang, , China

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Shijiazhuang, , China

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Suzhou, , China

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Taiyuan, , China

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Tianjin, , China

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Wuhan, , China

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Xi'an, , China

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Yangzhou, , China

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Yichang, , China

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Brno, , Czechia

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Hodonín, , Czechia

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Hradec Králové, , Czechia

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Hranice, , Czechia

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Karlovy Vary, , Czechia

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Kladno, , Czechia

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Kolín, , Czechia

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Litomyšl, , Czechia

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Mladá Boleslav, , Czechia

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Olomouc, , Czechia

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Plze?-Bory, , Czechia

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Prague, , Czechia

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Praha 8 - Libe?, , Czechia

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Slaný, , Czechia

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Teplice, , Czechia

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Uherské Hradišt?, , Czechia

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Valašské Mezi?í?í, , Czechia

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Esbjerg, , Denmark

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Herlev, , Denmark

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Hjørring, , Denmark

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Hvidovre, , Denmark

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Køge, , Denmark

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Tallinn, , Estonia

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Besançon, , France

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Bron, , France

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Chambray-lès-Tours, , France

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Corbeil-Essonnes, , France

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Lille, , France

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Montpellier, , France

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Nantes, , France

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Nice, , France

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Pau, , France

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Rouen, , France

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Toulouse, , France

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Vandœuvre-lès-Nancy, , France

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Berlin, , Germany

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Bielefeld, , Germany

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Bonn, , Germany

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Coburg, , Germany

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Dresden, , Germany

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Halle, , Germany

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Hamburg, , Germany

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Heidelberg, , Germany

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Konstanz, , Germany

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Langen, , Germany

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Leipzig, , Germany

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Ludwigshafen, , Germany

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Magdeburg, , Germany

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Mainz, , Germany

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Markkleeberg, , Germany

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Papenburg, , Germany

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Stuttgart, , Germany

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Ulm, , Germany

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Witten, , Germany

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Athens, , Greece

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Heraklion -Crete, , Greece

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Larissa, , Greece

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Thessalonikis, , Greece

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Voula, , Greece

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Balatonfüred, , Hungary

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Berettyóújfalu, , Hungary

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Budapest, , Hungary

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Győr, , Hungary

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Miskolc, , Hungary

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Nagykanizsa, , Hungary

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Szekszárd, , Hungary

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Székesfehérvár, , Hungary

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Szolnok, , Hungary

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Zalaegerszeg, , Hungary

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Aichi, , Japan

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Chiba, , Japan

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Chikushino-shi, , Japan

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Ehime, , Japan

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Fukuoka, , Japan

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Gifu, , Japan

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Gunma, , Japan

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Hatsukaichi, , Japan

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Hitachi, , Japan

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Hokkaido, , Japan

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Hyōgo, , Japan

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Ibaraki, , Japan

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Ishikawa, , Japan

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Izumo, , Japan

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Kagawa, , Japan

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Kahoku-District, , Japan

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Kanagawa, , Japan

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Kobe, , Japan

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Komatsushima-shi, , Japan

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Koshigaya-shi, , Japan

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Kumamoto, , Japan

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Kyoto, , Japan

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Miyazaki, , Japan

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Nagano, , Japan

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Nagasaki, , Japan

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Nagoya, , Japan

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Niigata, , Japan

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Okayama, , Japan

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Okinawa, , Japan

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Osaka, , Japan

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Ōita, , Japan

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Saga, , Japan

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Saitama, , Japan

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Sapporo, , Japan

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Sendai, , Japan

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Shiga, , Japan

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Shimane, , Japan

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Shizuoka, , Japan

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Tachikawa, , Japan

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Takaraduka, , Japan

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Tochigi, , Japan

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Tokushima, , Japan

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Tokyo, , Japan

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Toyama, , Japan

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Toyoake, , Japan

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Tsu, , Japan

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Wakayama, , Japan

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Yamaguchi, , Japan

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Yatsushiro, , Japan

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Yokohama, , Japan

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Yonago, , Japan

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Daugavpils, , Latvia

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Kuldīga, , Latvia

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Liepāja, , Latvia

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Riga, , Latvia

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Sigulda, , Latvia

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Ventspils, , Latvia

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Alytus, , Lithuania

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Kaunas, , Lithuania

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Klaipėda, , Lithuania

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Panevezys, , Lithuania

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Šiauliai, , Lithuania

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Vilnius, , Lithuania

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Cheras, , Malaysia

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George Town, , Malaysia

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Johor Bahru, , Malaysia

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Kota Kinabalu, , Malaysia

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Culiacán, , Mexico

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Durango, , Mexico

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Guadalajara, , Mexico

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León, , Mexico

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Mexico City, , Mexico

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México, , Mexico

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Oaxaca City, , Mexico

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Pachuca, , Mexico

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Puebla City, , Mexico

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Querétaro, , Mexico

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San Luis Potosí City, , Mexico

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Tampico, , Mexico

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Veracruz, , Mexico

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Almere Stad, , Netherlands

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Amsterdam, , Netherlands

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Blaricum, , Netherlands

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Breda, , Netherlands

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Deventer, , Netherlands

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Doetinchem, , Netherlands

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Ede, , Netherlands

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Groningen, , Netherlands

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Heerlen, , Netherlands

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Helmond, , Netherlands

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Maastricht, , Netherlands

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Meppel, , Netherlands

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Tilburg, , Netherlands

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Będzin, , Poland

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Gdynia, , Poland

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Gliwice, , Poland

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Grodzisk Mazowiecki, , Poland

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Inowrocław, , Poland

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Katowice, , Poland

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Kielce, , Poland

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Krakow, , Poland

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Kutno, , Poland

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Lodz, , Poland

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Lubin, , Poland

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Lublin, , Poland

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Myślenice, , Poland

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Olsztyn, , Poland

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Ostrowiec Świętokrzyski, , Poland

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Ostrołęka, , Poland

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Oświęcim, , Poland

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Puławy, , Poland

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Płock, , Poland

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Rabka-Zdrój, , Poland

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Skierniewice, , Poland

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Starogard Gdański, , Poland

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Szczecin, , Poland

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Torun, , Poland

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Warsaw, , Poland

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Wroclaw, , Poland

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Włocławek, , Poland

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Zabrze, , Poland

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Zamość, , Poland

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Łódż, , Poland

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Almada, , Portugal

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Aveiro, , Portugal

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Braga, , Portugal

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Carnaxide, , Portugal

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Coimbra, , Portugal

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Covilha, , Portugal

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Leiria, , Portugal

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Lisbon, , Portugal

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Matosinhos Municipality, , Portugal

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Viana do Castelo, , Portugal

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Vila Real, , Portugal

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Bacau, , Romania

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Baia Mare, , Romania

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Brasov, , Romania

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Brăila, , Romania

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Bucharest, , Romania

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Buzău, , Romania

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Cluj-Napoca, , Romania

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Craiova, , Romania

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Focşani, , Romania

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Galati, , Romania

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Iași, , Romania

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Oradea, , Romania

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Piteşti, , Romania

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Sibiu, , Romania

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Târgu Mureş, , Romania

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Timișoara, , Romania

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Arkhangelsk, , Russia

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Barnaul, , Russia

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Chita, , Russia

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Ivanovo, , Russia

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Izhevsk, , Russia

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Kaluga, , Russia

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Kemerovo, , Russia

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Kirov, , Russia

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Krasnoyarsk, , Russia

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Kursk, , Russia

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Moscow, , Russia

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Moscow, Zelenograd, , Russia

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Nizhny Novgorod, , Russia

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Novosibirsk, , Russia

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Orenburg, , Russia

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Perm, , Russia

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Rostov-on-Don, , Russia

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Ryazan, , Russia

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Saint Petersburg, , Russia

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Samara, , Russia

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Saratov, , Russia

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Syktyvkar, , Russia

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Tomsk, , Russia

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Tyumen, , Russia

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Voronezh, , Russia

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Yaroslavl, , Russia

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Yekaterinburg, , Russia

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Banská Bystrica, , Slovakia

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Bardejov, , Slovakia

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Košice, , Slovakia

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Lučenec, , Slovakia

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Moldava nad Bodvou, , Slovakia

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Nitra, , Slovakia

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Považská Bystrica, , Slovakia

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Svidník, , Slovakia

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Bloemfontein, , South Africa

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Cape Town, , South Africa

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Centurion, , South Africa

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Durban, , South Africa

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Pinelands, , South Africa

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Pretoria, , South Africa

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Tongaat, , South Africa

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Busan, , South Korea

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Cheongju-si, , South Korea

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Daegu, , South Korea

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Daejeon, , South Korea

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Gwangju, , South Korea

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Seongnam-si, , South Korea

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Seoul, , South Korea

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Wŏnju, , South Korea

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A Coruña, , Spain

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Alicante, , Spain

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Almería, , Spain

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Ávila, , Spain

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Barcelona, , Spain

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Burgos, , Spain

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Cáceres, , Spain

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Elche, , Spain

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Granada, , Spain

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Lorca, , Spain

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Madrid, , Spain

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Majadahonda, , Spain

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Murcia, , Spain

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Olot, , Spain

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Orihuela, , Spain

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Palma de Mallorca, , Spain

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San Juan, , Spain

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Sanlúcar de Barrameda, , Spain

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Sant Joan Despí, , Spain

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Santander, , Spain

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Seville, , Spain

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Terrassa, , Spain

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Torrevieja, , Spain

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Valencia, , Spain

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Vigo, , Spain

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Viladecans, , Spain

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Falun, , Sweden

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Jönköping, , Sweden

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Ljungby, , Sweden

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Stockholm, , Sweden

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Uppsala, , Sweden

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Ankara, , Turkey (Türkiye)

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Bursa, , Turkey (Türkiye)

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Diyarbakır, , Turkey (Türkiye)

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Eskişehir, , Turkey (Türkiye)

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Istanbul, , Turkey (Türkiye)

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Kahramanmaraş, , Turkey (Türkiye)

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Kocaeli, , Turkey (Türkiye)

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Konya, , Turkey (Türkiye)

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Kırıkkale, , Turkey (Türkiye)

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Mersin, , Turkey (Türkiye)

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Sivas, , Turkey (Türkiye)

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Cherkassy, , Ukraine

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Cherkasy, , Ukraine

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Dnipro, , Ukraine

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Donetsk, , Ukraine

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Kharkiv, , Ukraine

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Kyiv, , Ukraine

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Lutsk, , Ukraine

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Lviv, , Ukraine

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Odesa, , Ukraine

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Poltava, , Ukraine

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Sumy, , Ukraine

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Vinnitsa, , Ukraine

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Vinnytsia, , Ukraine

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Zaporizhzhia, , Ukraine

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Zaporizhzhya, , Ukraine

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Zhytomyr, , Ukraine

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Aberdeen, , United Kingdom

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Airdrie, , United Kingdom

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Birmingham, , United Kingdom

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Chesterfield, , United Kingdom

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Chichester, , United Kingdom

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Clydebank, , United Kingdom

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Cottingham, , United Kingdom

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Dudley, , United Kingdom

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Dundee, , United Kingdom

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East Kilbride, , United Kingdom

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Exeter, , United Kingdom

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Inverness, , United Kingdom

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Manchester, , United Kingdom

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Metropolitan Borough of Wirral, , United Kingdom

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TA1 5DA, , United Kingdom

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Countries

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United States Argentina Australia Brazil Bulgaria Canada China Czechia Denmark Estonia France Germany Greece Hungary Japan Latvia Lithuania Malaysia Mexico Netherlands Poland Portugal Romania Russia Slovakia South Africa South Korea Spain Sweden Turkey (Türkiye) Ukraine United Kingdom

References

Explore related publications, articles, or registry entries linked to this study.

Sharma A, Caldeira D, Razaghizad A, Pinto FJ, van Veldhuisen DJ, Mehra MR, Lam CSP, Cleland J, Anker SD, Greenberg B, Ferreira JP, Zannad F. Cardiovascular effects of rivaroxaban in heart failure patients with sinus rhythm and coronary disease with and without diabetes: a retrospective international cohort study from COMMANDER-HF. BMJ Open. 2023 Aug 11;13(8):e068865. doi: 10.1136/bmjopen-2022-068865.

Reference Type DERIVED
PMID: 37567750 (View on PubMed)

Ferreira JP, Cleland JG, Lam CSP, Anker SD, Mehra MR, van Veldhuisen DJ, Byra WM, La Police DA, Pitt B, Greenberg B, Zannad F. Heart failure re-hospitalizations and subsequent fatal events in coronary artery disease: insights from COMMANDER-HF, EPHESUS, and EXAMINE. Clin Res Cardiol. 2021 Oct;110(10):1554-1563. doi: 10.1007/s00392-021-01830-1. Epub 2021 Mar 8.

Reference Type DERIVED
PMID: 33686472 (View on PubMed)

Ferreira JP, Cleland JGF, Lam CSP, van Veldhuisen DJ, Byra WM, La Police DA, Anker SD, Mehra MR, Leroy C, Eschwege V, Toussaint-Hacquard M, Rossignol P, Greenberg B, Zannad F. Impact of Geographic Region on the COMMANDER-HF Trial. JACC Heart Fail. 2021 Mar;9(3):201-211. doi: 10.1016/j.jchf.2020.11.007. Epub 2021 Feb 3.

Reference Type DERIVED
PMID: 33549557 (View on PubMed)

Cunningham JW, Ferreira JP, Deng H, Anker SD, Byra WM, Cleland JGF, Gheorghiade M, Lam CSP, La Police D, Mehra MR, Neaton JD, Spiro TE, van Veldhuisen DJ, Greenberg B, Zannad F. Natriuretic Peptide-Based Inclusion Criteria in a Heart Failure Clinical Trial: Insights From COMMANDER HF. JACC Heart Fail. 2020 May;8(5):359-368. doi: 10.1016/j.jchf.2019.12.009. Epub 2020 Mar 11.

Reference Type DERIVED
PMID: 32171760 (View on PubMed)

Mehra MR, Vaduganathan M, Fu M, Ferreira JP, Anker SD, Cleland JGF, Lam CSP, van Veldhuisen DJ, Byra WM, Spiro TE, Deng H, Zannad F, Greenberg B. A comprehensive analysis of the effects of rivaroxaban on stroke or transient ischaemic attack in patients with heart failure, coronary artery disease, and sinus rhythm: the COMMANDER HF trial. Eur Heart J. 2019 Nov 21;40(44):3593-3602. doi: 10.1093/eurheartj/ehz427.

Reference Type DERIVED
PMID: 31461239 (View on PubMed)

Greenberg B, Neaton JD, Anker SD, Byra WM, Cleland JGF, Deng H, Fu M, La Police DA, Lam CSP, Mehra MR, Nessel CC, Spiro TE, van Veldhuisen DJ, Vanden Boom CM, Zannad F. Association of Rivaroxaban With Thromboembolic Events in Patients With Heart Failure, Coronary Disease, and Sinus Rhythm: A Post Hoc Analysis of the COMMANDER HF Trial. JAMA Cardiol. 2019 Jun 1;4(6):515-523. doi: 10.1001/jamacardio.2019.1049.

Reference Type DERIVED
PMID: 31017637 (View on PubMed)

Zannad F, Anker SD, Byra WM, Cleland JGF, Fu M, Gheorghiade M, Lam CSP, Mehra MR, Neaton JD, Nessel CC, Spiro TE, van Veldhuisen DJ, Greenberg B; COMMANDER HF Investigators. Rivaroxaban in Patients with Heart Failure, Sinus Rhythm, and Coronary Disease. N Engl J Med. 2018 Oct 4;379(14):1332-1342. doi: 10.1056/NEJMoa1808848. Epub 2018 Aug 27.

Reference Type DERIVED
PMID: 30146935 (View on PubMed)

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

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RIVAROXHFA3001

Identifier Type: OTHER

Identifier Source: secondary_id

2013-000046-19

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CR101940

Identifier Type: -

Identifier Source: org_study_id

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