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Trials / Completed

CompletedNCT01756612

A Study to Assess Hemoglobin Level Depending on the Comorbidity Index in Chronic Kidney Disease (CKD) Participants Not in Dialysis Treated With Methoxy Polyethylene Glycol-Epoetin Beta (COMETE)

A Non-interventional Study to Assess the Hemoglobin Level Depending on the Comorbidity Index in Chronic Kidney Disease (CKD) Patients Not in Dialysis Treated With Mircera®

Status
Completed
Phase
Study type
Observational
Enrollment
551 (actual)
Sponsor
Hoffmann-La Roche · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This prospective, multicenter, observational study will evaluate the impact of comorbidity factors on the hemoglobin level in participants with chronic kidney disease who are not on dialysis and initiated on treatment with methoxy polyethylene glycol-epoetin beta (Mircera). Data will be collected for 9 months after initiation of methoxy polyethylene glycol-epoetin beta treatment.

Conditions

Interventions

TypeNameDescription
DRUGMethoxy Polyethylene Glycol-Epoetin BetaMethoxy polyethylene glycol-epoetin beta will be administered at the discretion of treating physician. Study protocol does not specify any treatment regimen.

Timeline

Start date
2012-11-21
Primary completion
2015-03-25
Completion
2015-03-25
First posted
2012-12-27
Last updated
2019-07-15

Locations

108 sites across 1 country: France

Source: ClinicalTrials.gov record NCT01756612. Inclusion in this directory is not an endorsement.

A Study to Assess Hemoglobin Level Depending on the Comorbidity Index in Chronic Kidney Disease (CKD) Participants Not i (NCT01756612) · Clinical Trials Directory