Clinical trial
The Safety and Efficacy of the Buprenorphine Transdermal Delivery System in…
NCT00315887 · Purdue Pharma LP, Industry · Completed
Key facts
| NCT number | NCT00315887 |
|---|---|
| Title | The Safety and Efficacy of the Buprenorphine Transdermal Delivery System in Subjects With Chronic Back Pain. |
| Official title | A Double-Blind Comparative Study of Buprenorphine Transdermal System (BTDS) and Hydrocodone/Acetaminophen Tablets in Patients With Chronic Back Pain |
| Lead sponsor | Purdue Pharma LP, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Chronic Low Back Pain |
| Intervention type | Drug |
| Interventions | Buprenorphine transdermal delivery system |
| Enrollment | 250 |
| Start date | Apr 1, 1999 |
| Completion | Oct 1, 1999 |
| First posted | Apr 19, 2006 |
| Last update posted | May 3, 2006 |
| Countries | United States |
At a glance
- 10–99 Study sites
- No 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: