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Clinical Trial Summary

This study is to document the time spent by health care personnel on anemia-related tasks, including preparation, distribution and administration of monopegylated epoetin beta (Mircera) or other erythropoiesis-stimulating agents (ESAs) in patients with end stage renal disease in hemodialysis centers in Croatia. The total average time will be determined for the same number of patients on monopegylated epoetin beta and patients on other ESAs. In addition, qualitative information will be obtained on changes in practice patterns that may have occurred with the introduction of monopegylated epoetin beta.


Clinical Trial Description

n/a


Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02625844
Study type Observational
Source Hoffmann-La Roche
Contact
Status Completed
Phase N/A
Start date September 2011
Completion date August 2012

See also
  Status Clinical Trial Phase
Completed NCT01756612 - 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)
Completed NCT04885647 - A Study of YPEG-rhEPO in Patients Suffered From Anemia Due to Chronic Kidney Disease Phase 2
Completed NCT02596945 - Observational Study of Methoxy Polyethylene Glycol Epoetin Beta Daily Use in Participants on Peritoneal Dialysis N/A
Completed NCT02540213 - Observational Study of MIRCERA in Users of Self-Application and Multidose Systems N/A