Nabilone for the Treatment of Phantom Limb Pain

Phase 2

Completed

• Conditions: Phantom Limb Pain; Neuropathic Pain

• Registration Number: NCT00699634
• Lead Sponsor: University of Manitoba

Brief Summary

The purpose of this proposed study is to conduct a randomized double-blind placebo controlled trial assessing the benefit of nabilone in pain management and improvement of quality of life in patients with phantom limb pain.

Our Hypothesis is that the synthetic cannabinoid Nabilone will significantly reduce the phantom limb pain and improve quality of life, compared to the placebo controlled group. This will be evident by finding significant differences in Visual Analogue Scale pain scores, frequency of phantom pain episodes, the Depression, Anxiety and Stress Scale, and the Groningen Sleep Quality Scale and daily prosthetic wearing time.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2008-06-17
• Study First Submitted QC: 2008-06-17
• Study First Posted: 2008-06-18
• Study Start: 2009-01
• Primary Completion: 2011-02
• Status Verified: 2011-04
• Study Completion: 2011-04
• Last Update Submitted: 2011-04-28
• Last Update Posted: 2011-04-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• The patient has been diagnosed with phantom limb pain by a Rehabilitation Medicine Specialist.
• 18-70 years old.
• Any gender.
• The patient has not had resolution of their phantom limb pain with other treatments, such as a tricyclic antidepressant, or anticonvulsant medication.
• No previous use of oral cannabinoids for pain management.

Exclusion Criteria

• The patient's pain is better explained by a treatable cause of stump pain, such as neuroma or bony overgrowth.
• Gross abnormalities on routine baseline blood work including electrolytes, urea and creatinine, a complete blood count, and liver function tests (AST ALT GGT, Alk Phos, and LDH) that are twice the limit of normal. Normal tests taken within 3 months prior to the study will be accepted if there is no history of acute illness since the time the blood was drawn.
• Heart disease. (Cannabinoids can reduce heart rate and blood pressure) Patients with heart disease will be excluded based on a history of symptomatic angina, MI or CHF as well as a clinical exam.
• Schizophrenia or other Psychotic disorder
• Severe liver dysfunction.
• History of untreated non-psychotic emotional disorders.
• Cognitive impairment.
• Major illness in another body area.
• Pregnancy.
• Nursing mothers.
• History of drug dependency.
• A known sensitivity to marijuana or other cannabinoid agents

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Visual Analogue Scale for Pain	Baseline, 2, 4 and 6 weeks

Secondary Outcome Measures

Name	Time	Method
Depression Anxiety and Stress Scale	Baseline, 2, 4 and 6 weeks
Groningen Sleep Quality Scale	Baseline, 2, 4 and 6 weeks
SF-36	Baseline, 2, 4 and 6 weeks
Frequency of phantom limb pain	Baseline, 2, 4 and 6 weeks
Daily prosthetic wearing time	Baseline, 2, 4 and 6 weeks

Trial Locations

Locations (1)

Rehabilitation Hospital; 🇨🇦 Winnipeg, Manitoba, Canada