Clinical trial
Safety and Efficacy of Buprenorphine Transdermal System (BTDS) in Subjects With…
NCT00313014 · Purdue Pharma LP, Industry · Terminated
Key facts
| NCT number | NCT00313014 |
|---|---|
| Title | Safety and Efficacy of Buprenorphine Transdermal System (BTDS) in Subjects With Moderate to Severe Low Back Pain |
| Official title | A Multicenter, Randomized, Double-blind, Active Comparator Study to Determine the Efficacy and Safety of BTDS 20 or Oxycodone Immediate-release Versus BTDS 5 in Subjects With Moderate to Severe Low Back Pain |
| Lead sponsor | Purdue Pharma LP, Industry |
| Status | Terminated |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Back Pain Lower Back Chronic |
| Intervention type | Drug |
| Interventions | Buprenorphine, Oxycodone Immediate-Release |
| Enrollment | 660 |
| Start date | Feb 1, 2004 |
| Primary completion | Sep 1, 2005 |
| Completion | Sep 1, 2005 |
| First posted | Apr 11, 2006 |
| Last update posted | Sep 3, 2012 |
| Countries | United States |
At a glance
- 10–99 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: