A Retrospective Observational Study of Hemoglobin Levels in Patients With Renal Anemia Treated With Mircera (Methoxy Polyethylene Glycol-Epoetin Beta)

NCT ID: NCT01379963

Last Updated: 2017-07-13

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

Total Enrollment

780 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-04-30

Study Completion Date

2011-02-28

Brief Summary

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

This retrospective observational study will evaluate the hemoglobin levels in patients with renal anemia over 6 months treatment with Mircera (methoxy polyethylene glycol-epoetin beta).

Detailed Description

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

Conditions

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

Anemia, Kidney Disease, Chronic

Study Design

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

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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

Cohort

No interventions assigned to this group

Eligibility Criteria

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

Inclusion Criteria

* Adult patients, \>/= 18 years of age
* Renal anemia treated with Mircera for at least 6 months before entering study

Exclusion Criteria

* Patients who refuse or are incapable of giving their written informed consent to retrospective data collection
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.

Hoffmann-La Roche

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.

Clinical Trials

Role: STUDY_DIRECTOR

Hoffmann-La Roche

Locations

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

Timios Stavros Clinic; Nephrology Department

Aigáleo, , Greece

Site Status

General Hospital of Artas; Nephrology

Arta, , Greece

Site Status

Pantokrator Private Clinic; Nephrology

Athens, , Greece

Site Status

Attikon Center; Nephrology

Athens, , Greece

Site Status

Athinaiki Private Clinic

Athens, , Greece

Site Status

Kyanos Stavros Private Hospital; Nephrologic Clinic

Athens, , Greece

Site Status

Iaso General Private Clinic; Nephrology

Athens, , Greece

Site Status

Iatriko Athinon Clinic Dafnis; Nephrology Department

Daphni-athens, , Greece

Site Status

Kyanous Stavros of Patras, Renal Disease Therapy Unit

Pátrai, , Greece

Site Status

Olympion Therapeytirion; Nefrology

Pátrai, , Greece

Site Status

Iasis Private Clinic

Piraeus, , Greece

Site Status

General Hospital Of Chalkidikis; Dialysis Center Unit

Polygyros, , Greece

Site Status

Diavalkaniko Kentro; Nephrology

Thessaloniki, , Greece

Site Status

General Hospital of Thessalonikis G.Papanikolaou; Nephrology

Thessaloniki, , Greece

Site Status

Alfa Nefrodynamiki; Nefrology

Thessaloniki, , Greece

Site Status

Thessaliki Nossileytiki; Nephrology

Volos, , Greece

Site Status

General Hospital of Volos; Nephrology

Volos, , Greece

Site Status

Countries

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

Greece

Other Identifiers

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

ML22014

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.