XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HBR Patients.

NCT ID: NCT03218787

Last Updated: 2021-11-05

Study Results

Results available

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

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

2047 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-07-19

Study Completion Date

2020-09-04

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

XIENCE 90 study is a prospective, single arm, multi-center, open label trial to evaluate the safety of 3-month dual antiplatelet therapy (DAPT) in subjects at high risk of bleeding (HBR) undergoing percutaneous coronary intervention (PCI) with the approved XIENCE family of coronary drug-eluting stents.

The XIENCE family stent systems include commercially approved XIENCE Xpedition Everolimus Eluting Coronary Stent System (EECSS), XIENCE Alpine EECSS, XIENCE PRO\^X EECSS \[rebrand of the XIENCE Xpedition Stent System and is only available outside of the United States (OUS)\], XIENCE PRO\^A EECSS (rebrand of the XIENCE Alpine Stent System and is only available OUS) and XIENCE Sierra EECSS of coronary drug-eluting stents.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

A. Primary Objective:

To show non-inferiority of the primary endpoint of all death or all MI (modified ARC) from 3 to 12 months following XIENCE implantation in HBR subjects treated with 3-month DAPT compared to a historical control after propensity score adjustment.

B. Secondary Objective:

* To show superiority of the major secondary endpoint of major bleeding (Bleeding Academic Research Consortium \[BARC\] type 2-5) from 3 to 12 months following XIENCE implantation in HBR subjects treated with 3-month DAPT compared to a historical control after propensity score adjustment.
* To evaluate stent thrombosis (ARC definite/probable) from 3 to 12 months following XIENCE implantation in HBR subjects treated with 3-month DAPT against a performance goal (PG).

All registered subjects will be followed at 3, 6 and 12 months post index procedure.

The data collected from this study will be compared with the historical control of non-complex HBR subjects treated with standard DAPT duration of up to 12 months from the XIENCE V USA study, which is a US post-approval study to evaluate the safety of XIENCE V EECSS in "all-comer" population under real-world setting.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Coronary Artery Lesions

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Coronary Artery Lesions XIENCE Dual Antiplatelet Therapy (DAPT) Reduced DAPT Risk of bleeding Drug-eluting stents

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

XIENCE

Subjects will receive XIENCE family stents and if a subject was DAPT compliant and event free, then took 3 month DAPT, following with aspirin mono-therapy until 12 month

Group Type EXPERIMENTAL

XIENCE

Intervention Type DEVICE

Subjects who received XIENCE family stent systems will be included.

DAPT

Intervention Type DRUG

3-month clear subjects who receive 3-month DAPT without interruption of either aspirin and/or P2Y12 receptor inhibitor for \> 7 consecutive days.

Subject who are "3-month clear" will discontinue P2Y12 inhibitor after 3-month visit, but continue taking aspirin through 12-month follow-up. Subjects who are not eligible for early P2Y12 inhibitor discontinuation will be treated per site standard of care.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

XIENCE

Subjects who received XIENCE family stent systems will be included.

Intervention Type DEVICE

DAPT

3-month clear subjects who receive 3-month DAPT without interruption of either aspirin and/or P2Y12 receptor inhibitor for \> 7 consecutive days.

Subject who are "3-month clear" will discontinue P2Y12 inhibitor after 3-month visit, but continue taking aspirin through 12-month follow-up. Subjects who are not eligible for early P2Y12 inhibitor discontinuation will be treated per site standard of care.

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Dual antiplatelet therapy

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Subject is considered at high risk for bleeding (HBR), defined as meeting one or more of the following criteria at the time of registration and in the opinion of the referring physician, the risk of major bleeding with \> 3-month DAPT outweighs the benefit:

1. ≥ 75 years of age.
2. Clinical indication for chronic (at least 6 months) or lifelong anticoagulation therapy.
3. History of major bleeding which required medical attention within 12 months of the index procedure.
4. History of stroke (ischemic or hemorrhagic).
5. Renal insufficiency (creatinine ≥ 2.0 mg/dl) or failure (dialysis dependent).
6. Systemic conditions associated with an increased bleeding risk (e.g. hematological disorders, including a history of or current thrombocytopenia defined as a platelet count \<100,000/mm\^3, or any known coagulation disorder associated with increased bleeding risk).
7. Anemia with hemoglobin \< 11g/dl.
2. Subject must be at least 18 years of age.
3. Subject or a legally authorized representative must provide written informed consent as approved by the Institutional Review Board (IRB)/Ethics Committee (EC) of the respective clinical site prior to any study related procedure.
4. Subject is willing to comply with all protocol requirements, including agreement to stop taking P2Y12 inhibitor at 3 months, if eligible per protocol.
5. Subject must agree not to participate in any other clinical trial for a period of one year following the index procedure.


1. Up to three target lesions with a maximum of two target lesions per epicardial vessel. Note:

* The definition of epicardial vessels means left anterior descending coronary artery (LAD), left circumflex coronary artery (LCX) and right coronary artery (RCA) and their branches. For example, the patient must not have \>2 lesions requiring treatment within both the LAD and a diagonal branch in total.
* If there are two target lesions within the same epicardial vessel, the two target lesions must be at least 15 mm apart per visual estimation; otherwise this is considered as a single target lesion.
2. Target lesion ≤ 32 mm in length by visual estimation.
3. Target lesion must be located in a native coronary artery with visually estimated reference vessel diameter between 2.25 mm and 4.25 mm.
4. Exclusive use of XIENCE family of stent systems during the index procedure.
5. Target lesion has been treated successfully, which is defined as achievement of a final in-stent residual diameter stenosis of \<20% with final TIMI-3 flow assessed by online quantitative angiography or visual estimation, with no residual dissection NHLBI grade ≥ type B, and no transient or sustained angiographic complications (e.g., distal embolization, side branch closure), no chest pain lasting \> 5 minutes, and no ST segment elevation \> 0.5 mm or depression lasting \> 5 minutes.

Exclusion Criteria

1. Subject with an indication for the index procedure of acute ST-segment elevation MI (STEMI).
2. Subject has a known hypersensitivity or contraindication to aspirin, heparin/bivalirudin, P2Y12 inhibitors (clopidogrel/prasugrel/ticagrelor), everolimus, cobalt, chromium, nickel, tungsten, acrylic and fluoro polymers or contrast sensitivity that cannot be adequately pre-medicated.
3. Subject with implantation of another drug-eluting stent (other than XIENCE) within 9 months prior to index procedure.
4. Subject has a known left ventricular ejection fraction (LVEF) \<30%.
5. Subject judged by physician as inappropriate for discontinuation from P2Y12 inhibitor use at 3 months, due to another condition requiring chronic P2Y12 inhibitor use.
6. Subject with planned surgery or procedure necessitating discontinuation of P2Y12 inhibitor within 3 months following index procedure.
7. Subject with a current medical condition with a life expectancy of less than 12 months.
8. Subject intends to participate in an investigational drug or device trial within 12 months following the index procedure.
9. Pregnant or nursing subjects and those who plan pregnancy in the period up to 1 year following index procedure. Female subjects of child-bearing potential must have a negative pregnancy test done within 7 days prior to the index procedure per site standard test.

Note: Female patients of childbearing potential should be instructed to use safe contraception (e.g., intrauterine devices, hormonal contraceptives: contraceptive pills, implants, transdermal patches, hormonal vaginal devices, injections with prolonged release.) It is accepted, in certain cases, to include subjects having a sterilised regular partner or subjects using a double barrier contraceptive method. However, this should be explicitly justified in special circumstances arising from the study design, product characteristics and/or study population
10. Subject is part of a vulnerable population, defined as subject whose willingness to volunteer in a clinical investigation could be unduly influenced by the expectation, whether justified or not, of benefits associated with participation or of retaliatory response from senior members of a hierarchy in case of refusal to participate. Examples of populations which may contain vulnerable subjects include: individuals with lack of or loss of autonomy due to immaturity or through mental disability, persons in nursing homes, children, impoverished persons, subjects in emergency situations, ethnic minority groups, homeless persons, nomads, refugees, and those incapable of giving informed consent. Other vulnerable subjects include, for example, members of a group with a hierarchical structure such as university students, subordinate hospital and laboratory personnel, employees of the sponsor, members of the armed forces, and persons kept in detention.
11. Subject is currently participating in another clinical trial that has not yet completed its primary endpoint.


1. Target lesion is in a left main location.
2. Target lesion is located within an arterial or saphenous vein graft.
3. Target lesion is restenotic from a previous stent implantation.
4. Target lesion is a total occluded lesion (TIMI flow 0).
5. Target lesion contains thrombus as indicated in the angiographic images (per SYNTAX score thrombus definition).
6. Target lesion is implanted with overlapping stents, whether planned or for bailout.

Note: If there is more than one target lesion, all target lesions must satisfy the angiographic eligibility criteria. Non-target lesion (i.e., lesions that do not meet the angiographic criteria listed above) treatments are not allowed during the index procedure.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Abbott Medical Devices

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Roxana Mehran

Role: PRINCIPAL_INVESTIGATOR

Abbott Medical Devices

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Huntsville Hospital (Heart Center Research LLC)

Huntsville, Alabama, United States

Site Status

Scottsdale Healthcare Hospitals (d/b/a HonorHealth - HonorHealth Research Institute)

Scottsdale, Arizona, United States

Site Status

Arkansas Heart Hospital

Little Rock, Arkansas, United States

Site Status

John Muir Health Concord

Concord, California, United States

Site Status

Washington Hospital (Mission Cardiovascular Research Institute)

Fremont, California, United States

Site Status

Scripps Memorial Hospital/Prebys Cardiovascular Institute

La Jolla, California, United States

Site Status

Cedars-Sinai Medical Center

Los Angeles, California, United States

Site Status

University of California Davis Medical Center

Sacramento, California, United States

Site Status

Sharp Grossmont Hospital (La Mesa Cardiac Center)

San Diego, California, United States

Site Status

Sharp Memorial Hospital / San Diego Cardiac Center

San Diego, California, United States

Site Status

Santa Barbara Cottage Hospital/Sansum Clinic

Santa Barbara, California, United States

Site Status

Torrance Memorial Medical Center

Torrance, California, United States

Site Status

Rocky Mountain Regional VA Medical Center

Aurora, Colorado, United States

Site Status

Medstar Washington Hospital

Washington D.C., District of Columbia, United States

Site Status

JFK Medical Center

Atlantis, Florida, United States

Site Status

Clearwater Cardiovasular Consultants

Clearwater, Florida, United States

Site Status

Morton Plant Mease Healthcare System

Clearwater, Florida, United States

Site Status

North Florida Regional / The Cardiac and Vascular Institute

Gainesville, Florida, United States

Site Status

St. Vincent's Medical Center (St. Vincent's Healthcare)

Jacksonville, Florida, United States

Site Status

Tallahassee Memorial Hospital / Tallahassee Research Institute, Inc.

Tallahassee, Florida, United States

Site Status

University Health, INC/University Cardiology Associates, LLC

Augusta, Georgia, United States

Site Status

Augusta Medical Center

Augusta, Georgia, United States

Site Status

Atlanta Veterans Affairs Medical Center

Decatur, Georgia, United States

Site Status

North Georgia Heart Foundation, Inc.

Gainesville, Georgia, United States

Site Status

St. John's Hospital

Springfield, Illinois, United States

Site Status

Elkhart General Hospital/Midwest Cardiology Research & Education Foundation

Elkhart, Indiana, United States

Site Status

Franciscan Physician Network-Indiana Heart Physicians

Indianapolis, Indiana, United States

Site Status

St. Vincent Heart Center of Indiana

Indianapolis, Indiana, United States

Site Status

The University of Kansas Medical Center

Kansas City, Kansas, United States

Site Status

Cardiovascular Research Institute of Kansas/Via Christi Regional Medical

Wichita, Kansas, United States

Site Status

Kansas Heart Hospital (Cardiovascular Research Institute of Kansas)

Wichita, Kansas, United States

Site Status

University of Kentucky/Gill Heart and Vascular Institute

Lexington, Kentucky, United States

Site Status

Baptist Health Louisville/Louisville Cardiology

Louisville, Kentucky, United States

Site Status

Eastern Maine Medical Center/One Northeast Drive

Bangor, Maine, United States

Site Status

MedStar Union Memorial Hospital

Baltimore, Maryland, United States

Site Status

Massachusetts General Hospital

Boston, Massachusetts, United States

Site Status

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Site Status

Lahey Clinic/Lahey Hospital and Medical Center

Burlington, Massachusetts, United States

Site Status

Baystate Medical Center

Springfield, Massachusetts, United States

Site Status

McLaren Bay Region

Bay City, Michigan, United States

Site Status

St John Hospital & Medical Center

Detroit, Michigan, United States

Site Status

Genesys Regional Medical Center (Regional Cardiology Associates)

Grand Blanc, Michigan, United States

Site Status

Western Michigan University Homer Stryker M.D. School of Medicine

Kalamazoo, Michigan, United States

Site Status

MidMichigan Medical Center Midland

Midland, Michigan, United States

Site Status

Traverse Heart and Vascular Munson Medical Center

Traverse City, Michigan, United States

Site Status

St. Joseph Mercy Hospital (Michigan Heart)

Ypsilanti, Michigan, United States

Site Status

Abbott Northwestern Hospital (Minneapolis Heart Institute Foundation)

Minneapolis, Minnesota, United States

Site Status

CentraCare

Saint Cloud, Minnesota, United States

Site Status

St Dominic-Jackson Memorial Hospital (Jackson Heart Clinic)

Jackson, Mississippi, United States

Site Status

North Mississippi Medical Center (Cardiology Associates Research)

Tupelo, Mississippi, United States

Site Status

Boone Hospital Center (Missouri Cardiovascular Specialists)

Columbia, Missouri, United States

Site Status

St. Luke's Hospital/Mid America Heart Institute

Kansas City, Missouri, United States

Site Status

Washington University School of Medicine Barnes Jewish Hospital

St Louis, Missouri, United States

Site Status

St. Patrick Hospital International Heart Institute of Montana Foundation

Missoula, Montana, United States

Site Status

Bryan Local General Hospital (Bryan Medical Center East)

Lincoln, Nebraska, United States

Site Status

Our Lady of Lourdes/Cardiovascular Associates of the Delaware Valley (The Heart House)

Camden, New Jersey, United States

Site Status

Englewood Hospital and Medical Center

Englewood, New Jersey, United States

Site Status

Morristown Medical Center

Morristown, New Jersey, United States

Site Status

Jersey Shore University Medical Center

Neptune City, New Jersey, United States

Site Status

St. Joseph's Hospital Health Center

East Syracuse, New York, United States

Site Status

New York - Presbyterian Queens Lang Research Center

Flushing, New York, United States

Site Status

NYU Langone Health

New York, New York, United States

Site Status

Mount Sinai Medical Center

New York, New York, United States

Site Status

New York Presbyterian Hospital - Weill Cornell

New York, New York, United States

Site Status

Lenox Hill Hospital (Northwell)/ Feinstein Institute

New York, New York, United States

Site Status

Stony Brook University Medical Center

Stony Brook, New York, United States

Site Status

The Presbyterian Hospital (d/b/a Novant Health Heart and Vascular Institute) Novant Health Clinical Research

Charlotte, North Carolina, United States

Site Status

NC Heart and Vascular Research

Raleigh, North Carolina, United States

Site Status

Wake Forest Baptist Medical Center (Wake Forest University Health Sciences)/Medical Center Boulevard

Winston-Salem, North Carolina, United States

Site Status

University Hospitals Cleveland Medical Center

Cleveland, Ohio, United States

Site Status

Cardiovascular Research Center, LLC (Mercy Health St. Vincent Medical Center LLC)

Toledo, Ohio, United States

Site Status

Integris Baptist Medical Center/Integris Cardiovascular Physicians, LLC

Oklahoma City, Oklahoma, United States

Site Status

Hillcrest Medical Center (Oklahoma Heart Institute)

Tulsa, Oklahoma, United States

Site Status

Providence St. Vincent Medical Center

Portland, Oregon, United States

Site Status

Holy Spirit Hospital

Camp Hill, Pennsylvania, United States

Site Status

Doylestown Hospital

Doylestown, Pennsylvania, United States

Site Status

UPMC Hamot/Medicor Associates, Inc.,

Erie, Pennsylvania, United States

Site Status

Harrisburg Hospital/Pinnacle Health Cardiovascular Institute, Inc.

Harrisburg, Pennsylvania, United States

Site Status

St. Mary Medical Center

Langhorne, Pennsylvania, United States

Site Status

Penn Presbyterian Medical Center/Penn Heart and Vascular Pavilion,

Philadelphia, Pennsylvania, United States

Site Status

UPMC

Pittsburgh, Pennsylvania, United States

Site Status

Allegheny General Hospital

Pittsburgh, Pennsylvania, United States

Site Status

St. Joseph Medical Center

Wyomissing, Pennsylvania, United States

Site Status

Rhode Island Hospital

Providence, Rhode Island, United States

Site Status

AnMed Health Clinical Research

Anderson, South Carolina, United States

Site Status

Sanford Health

Sioux Falls, South Dakota, United States

Site Status

Erlanger Medical Center

Chattanooga, Tennessee, United States

Site Status

Wellmont Holston Valley Medical Center

Kingsport, Tennessee, United States

Site Status

Turkey Creek Medical Center (Knoxville HMA Cardiology, LLC)

Knoxville, Tennessee, United States

Site Status

Baptist Memorial Hospital

Memphis, Tennessee, United States

Site Status

Centennial Medical Center (TriStar Centennial Medical Center)

Nashville, Tennessee, United States

Site Status

Heart Hospital of Austin

Austin, Texas, United States

Site Status

Baylor Heart and Vascular Hospital

Dallas, Texas, United States

Site Status

Memorial Hermann-Hermann Hospital/UTHealth

Houston, Texas, United States

Site Status

Texas Tech University Health (University Medical Center)

Lubbock, Texas, United States

Site Status

East Texas Medical Center

Tyler, Texas, United States

Site Status

The University of Vermont Medical Center

Burlington, Vermont, United States

Site Status

Inova Fairfax Hospital/Inova Heart and Vascular Institute

Falls Church, Virginia, United States

Site Status

Mary Washington Hospital/Virginia Cardiovascular Consultants

Fredericksburg, Virginia, United States

Site Status

Providence Regional Medical Center Everett

Everett, Washington, United States

Site Status

Charleston Area Medical Center Memorial Division

Charleston, West Virginia, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

References

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

Valgimigli M, Cao D, Angiolillo DJ, Bangalore S, Bhatt DL, Ge J, Hermiller J, Makkar RR, Neumann FJ, Saito S, Picon H, Toelg R, Maksoud A, Chehab BM, Choi JW, Campo G, De la Torre Hernandez JM, Kunadian V, Sardella G, Thiele H, Varenne O, Vranckx P, Windecker S, Zhou Y, Krucoff MW, Ruster K, Zheng Y, Mehran R; XIENCE 90 and XIENCE 28 Investigators. Duration of Dual Antiplatelet Therapy for Patients at High Bleeding Risk Undergoing PCI. J Am Coll Cardiol. 2021 Nov 23;78(21):2060-2072. doi: 10.1016/j.jacc.2021.08.074.

Reference Type DERIVED
PMID: 34794687 (View on PubMed)

Valgimigli M, Cao D, Makkar RR, Bangalore S, Bhatt DL, Angiolillo DJ, Saito S, Ge J, Neumann FJ, Hermiller J, Picon H, Toelg R, Maksoud A, Chehab BM, Wang LJ, Wang J, Mehran R. Design and rationale of the XIENCE short DAPT clinical program: An assessment of the safety of 3-month and 1-month DAPT in patients at high bleeding risk undergoing PCI with an everolimus-eluting stent. Am Heart J. 2021 Jan;231:147-156. doi: 10.1016/j.ahj.2020.09.019. Epub 2020 Oct 6.

Reference Type DERIVED
PMID: 33031789 (View on PubMed)

Provided Documents

Download supplemental materials such as informed consent forms, study protocols, or participant manuals.

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

16-308

Identifier Type: -

Identifier Source: org_study_id