Viewing Study NCT01105494


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Study NCT ID: NCT01105494
Status: COMPLETED
Last Update Posted: 2012-09-13
First Post: 2010-04-14
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: An Observational Study of Epoetin Beta [Neorecormon] to Evaluate the Quality of Life in Patients on Dialysis With Chronic Renal Anemia
Sponsor: Hoffmann-La Roche
Organization:

Study Overview

Official Title: Prospective Study Evaluating the Quality of Life in Dialysis Patients With End Stage Renal Disease
Status: COMPLETED
Status Verified Date: 2011-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This multicenter, prospective, observational study will evaluate the quality of life and the factors that influence the quality of life of epoetin beta \[Neorecormon\] in patients with renal chronic anemia, who are on dialysis. For each eligible patient data will be collected for 6 months. Target sample size is 5000-7000 patients.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: