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Clinical trial

A 12-Week, Placebo Controlled, Double Blind, Randomized Withdrawal Study to Evaluate the Efficacy and Safety of Buprenorphine HCl Buccal Film in Subjects With Moderate to Severe Chronic Low Back Pain

NCT01256450 is registered in ClinicalTrials.gov with BioDelivery Sciences International as lead sponsor.

NCT NCT01256450
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Registry record

As filed in ClinicalTrials.gov.

Title
A 12-Week, Placebo Controlled, Double Blind, Randomized Withdrawal Study to Evaluate the Efficacy and Safety of Buprenorphine HCl Buccal Film in Subjects With Moderate to Severe Chronic Low Back Pain
Lead sponsor
BioDelivery Sciences International
Phase
Phase 3
Overall status
Completed
Start date
November 30, 2010
Completion date
July 31, 2011
Enrollment
334 (actual)
Sites
24

Conditions

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

low back pain, pain