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Lookup NU author(s): Dr Bernhard Frank, Joan Hughes, Professor John MatthewsORCiD, Dr Dilip Kapur
Objective To compare the analgesic efficacy and side effects of the synthetic cannabinoid nabilone with those of the weak opioid dihydrocodeine for chronic neuropathic pain. Design Randomised, double blind, crossover trial of 14 weeks' duration comparing dihydrocodeine and nabilone. Setting Outpatient units of three hospitals in the United Kingdom. Participants 96 patients with chronic neuropathic pain, aged 23-84 years. Main outcome measures The primary outcome was difference between nabilone and dihydrocodeine in pain, as measured by the mean visual analogue score computed over the last two weeks of each treatment period. Secondary outcomes were changes in mood, quality of life, steep, and psychometric function. Side effects were measured by a questionnaire. Intervention Patients received a maximum daily dose of 240 mg dihydrocodeine or 2 mg nabilone at the end of each escalating treatment period of 6 weeks. Treatment periods were separated by a 2 week washout period. Results Mean baseline visual analogue score was 69.6 mm (range 29.4-95.2) on a 0-100 mm scale. 73 patients were included in the available case analysis and 64 patients in the per protocol analysis. The mean score was 6.0 mm longer for nabilone than for dihydrocodeine (95% confidence interval 1.4 to 10.5) in the available case analysis and 5.6 mm (10.3 to 0.8) in the per protocol analysis. Side effects were more frequent with nabilone. Conclusion Dihydrococleine provided better pain relief than the synthetic cannabinoid nabilone and had slightly fewer side effects, although no major adverse events occurred for either drug. Trial registration Current Controlled Trials ISRCTNI5330757.
Author(s): Frank B, Serpell MG, Hughes J, Matthews JNS, Kapur D
Publication type: Article
Publication status: Published
Journal: British Medical Journal
Year: 2008
Volume: 336
Issue: 7637
Pages: 199-201
Date deposited: 20/05/2010
ISSN (print): 0959-535X
ISSN (electronic): 0959-8146
Publisher: BMJ Group
URL: http://dx.doi.org/10.1136/bmj.39429.619653.80
DOI: 10.1136/bmj.39429.619653.80
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