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A Study to Determine the Satisfaction With Actonel in Postmenopausal Women With Osteoporosis — ROSPA-CTx  

Osteoporosis, Postmenopausal Clinical Trial

Official title:
Multicenter and Prospective Study to Determine the Satisfaction With Actonel (Risedronate Sodium) 35mg Once a Week Using Biochemical Markers of Bone as a Control, in Postmenopausal Women With Osteoporosis

Clinical Trial Summary

The study in the labeled and real conditions of prescription of Actonel will investigate the satisfaction of patients with its new formulation: 35 mg Once A Week. The study will also measure response rates in CTX (the C-telopeptide of type I collagen) at baseline and after 12 weeks of treatment with risedronate 35 mg Once A Week.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00632216
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date May 2004
Completion date May 2006
View Details
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