Safety and Efficacy of Dose Conversion From Vicodin® to Buprenorphine Transdermal System (Butrans™) in Subjects With OA Pain
Clinical trial NCT00312572 · COMPLETED
Trial details
- NCT number
- NCT00312572
- Sponsor
- Purdue Pharma LP
- Status
- COMPLETED
- Phase
- Phase 3
- Study type
- INTERVENTIONAL
- Start date
- 2003-06-01
- Primary completion
- 2004-07-01
- Enrollment
- 204
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