Clinical trial

Efficacy and Safety Evaluation of Nabilone as Adjunctive Therapy to Gabapentin…

NCT00480181 · University of Manitoba, Other · Completed

Key facts

NCT number NCT00480181
Title Efficacy and Safety Evaluation of Nabilone as Adjunctive Therapy to Gabapentin for the Management of Neuropathic Pain in Multiple Sclerosis
Official title A Comparative, Single Center, Randomized, Double-blinded, Parallel, Placebo-controlled Study to Evaluate the Efficacy of Nabilone (Cesamet) as Adjunctive Therapy to Gabapentin (Neurontin) in the Management of Neuropathic Pain (NPP) Symptoms in Subjects With Multiple Sclerosis (MS)
Lead sponsor University of Manitoba, Other
Collaborators Bausch Health Americas, Inc. Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Neuropathic Pain, Multiple Sclerosis
Intervention type Drug, Other
Interventions nabilone, placebo
Enrollment 50
Start date Jun 1, 2007
Primary completion Jul 1, 2012
Completion Jul 1, 2012
First posted May 30, 2007
Last update posted Jul 27, 2012
Countries Canada

At a glance

  • 1–9 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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