Trials / Completed
CompletedNCT00460733
SOLID-Effect of Risedronate Sodium at Distal Radius in Colle's Fracture.
Local (Brazil) Study, Multicenter, Opened, Comparative, Randomized, With Parallel Groups, Phase IV, in Post Menopausal Woman With Colles' Fracture of the Risedronate Sodium Usage in the Consolidation and in the Callus of the Colles'Fracture.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 141 (actual)
- Sponsor
- Sanofi · Industry
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the efficacy and safety of risedronate sodium (Actonel®) after a wrist fracture in postmenopausal women.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Risedronate sodium | Actonel® 35 mg (risedronate sodium) and 1000 mg of calcium and 400 UI of Vitamine D3 |
| DRUG | Calcium & Vitamine D3 | 1000 mg of calcium and 400 UI of Vitamine D3 |
Timeline
- Start date
- 2007-03-01
- Primary completion
- 2011-09-01
- Completion
- 2011-09-01
- First posted
- 2007-04-16
- Last updated
- 2011-10-04
Locations
1 site across 1 country: Brazil
Source: ClinicalTrials.gov record NCT00460733. Inclusion in this directory is not an endorsement.