Low-dose vaporized cannabis significantly improves neuropathic pain
- PMID: 23237736
- PMCID: PMC3566631
- DOI: 10.1016/j.jpain.2012.10.009
Low-dose vaporized cannabis significantly improves neuropathic pain
Abstract
We conducted a double-blind, placebo-controlled, crossover study evaluating the analgesic efficacy of vaporized cannabis in subjects, the majority of whom were experiencing neuropathic pain despite traditional treatment. Thirty-nine patients with central and peripheral neuropathic pain underwent a standardized procedure for inhaling medium-dose (3.53%), low-dose (1.29%), or placebo cannabis with the primary outcome being visual analog scale pain intensity. Psychoactive side effects and neuropsychological performance were also evaluated. Mixed-effects regression models demonstrated an analgesic response to vaporized cannabis. There was no significant difference between the 2 active dose groups' results (P > .7). The number needed to treat (NNT) to achieve 30% pain reduction was 3.2 for placebo versus low-dose, 2.9 for placebo versus medium-dose, and 25 for medium- versus low-dose. As these NNTs are comparable to those of traditional neuropathic pain medications, cannabis has analgesic efficacy with the low dose being as effective a pain reliever as the medium dose. Psychoactive effects were minimal and well tolerated, and neuropsychological effects were of limited duration and readily reversible within 1 to 2 hours. Vaporized cannabis, even at low doses, may present an effective option for patients with treatment-resistant neuropathic pain.
Perspective: The analgesia obtained from a low dose of delta-9-tetrahydrocannabinol (1.29%) in patients, most of whom were experiencing neuropathic pain despite conventional treatments, is a clinically significant outcome. In general, the effect sizes on cognitive testing were consistent with this minimal dose. As a result, one might not anticipate a significant impact on daily functioning.
Published by Elsevier Inc.
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Comment in
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Marijuana for pain relief: don't jump to conclusions.J Pain. 2013 Oct;14(10):1250-1. doi: 10.1016/j.jpain.2013.07.002. J Pain. 2013. PMID: 24090991 No abstract available.
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Response to Stacey and Moller's letter to the editor.J Pain. 2013 Oct;14(10):1252-3. doi: 10.1016/j.jpain.2013.07.003. J Pain. 2013. PMID: 24090992 Free PMC article. No abstract available.
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