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Clinical trial

A Multicenter, Randomized, Double-blind, Active Comparator Study to Determine the Efficacy and Safety of BTDS 20 or Oxycodone Immediate-Release Vs Buprenorphine Transdermal System (BTDS) 5 in Subjects With Moderate to Severe Low Back Pain: A 52-Week Open-label Extension Phase of BUP3015

NCT01125917 is registered in ClinicalTrials.gov with Purdue Pharma LP as lead sponsor.

NCT NCT01125917
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Registry record

As filed in ClinicalTrials.gov.

Title
A Multicenter, Randomized, Double-blind, Active Comparator Study to Determine the Efficacy and Safety of BTDS 20 or Oxycodone Immediate-Release Vs Buprenorphine Transdermal System (BTDS) 5 in Subjects With Moderate to Severe Low Back Pain: A 52-Week Open-label Extension Phase of BUP3015
Lead sponsor
Purdue Pharma LP
Phase
Phase 3
Overall status
Terminated
Start date
June 30, 2004
Completion date
January 31, 2008
Enrollment
354 (actual)
Sites
84

Conditions

As the registry lists them; a condition with its own page is linked.

back pain lower back chronic