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Fosrenol Post-marketing Surveillance for Continuous Cyclic Peritoneal Dialysis in Japan — FOSRENOL-CAPD  

Hyperphosphatemia Clinical Trial

Official title:
Special Drug Use Investigation of Fosrenol (Investigation for Patients With Continuous Ambulatory Peritoneal Dialysis)

Clinical Trial Summary

This study is a regulatory post marketing surveillance in Japan, and it is a local prospective and observational study of patients in continuous ambulatory peritoneal dialysis (CAPD) who have received Fosrenol for hyperphosphatemia. The objective of this study is to assess safety and efficacy of using Fosrenol in clinical practice. This study is also all case investigation of which the enrollment period is one year, and all patients in CAPD who received Fosrenol for hyperphosphatemia will be recruited and followed one year.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01412398
Study type Observational
Source Bayer
Contact
Status Completed
Phase N/A
Start date April 7, 2009
Completion date September 1, 2016
View Details
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