drugset / Trial / NCT00632216
A Study to Determine the Satisfaction With Actonel in Postmenopausal Women With Osteoporosis
Non-randomizedSingle-groupOpen-labelTreatment
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.
Timeline
- Start
- 2004-05
- Primary completion
- —
- Completion
- 2006-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Risedronate | Small molecule | 35 mg | — |