# Buprenorphine Transdermal Patch in Subjects With Osteoarthritis Pain Requiring Opioids. Includes a 52-Week Safety Extension.

> **NCT00315458** · PHASE3 · TERMINATED · sponsor: **Purdue Pharma LP** · enrollment: 107 (actual)

## Conditions studied

- Osteoarthritis

## Interventions

- **DRUG:** Buprenorphine transdermal patch
- **DRUG:** Placebo transdermal patch

## Key facts

- **NCT ID:** NCT00315458
- **Lead sponsor:** Purdue Pharma LP
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2003-12
- **Primary completion:** 2005-03
- **Final completion:** 2005-03
- **Target enrollment:** 107 (ACTUAL)
- **Why stopped:** Administrative reasons.
- **Last updated:** 2012-09-03


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00315458

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00315458, "Buprenorphine Transdermal Patch in Subjects With Osteoarthritis Pain Requiring Opioids. Includes a 52-Week Safety Extension.". Retrieved via AI Analytics 2026-07-17 from https://api.ai-analytics.org/clinical/NCT00315458. Licensed CC0.

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