Skip to main content
AAN.com
Articles
February 12, 2007

Cannabis in painful HIV-associated sensory neuropathy
A randomized placebo-controlled trial

February 13, 2007 issue
68 (7) 515-521

Abstract

Objective: To determine the effect of smoked cannabis on the neuropathic pain of HIV-associated sensory neuropathy and an experimental pain model.
Methods: Prospective randomized placebo-controlled trial conducted in the inpatient General Clinical Research Center between May 2003 and May 2005 involving adults with painful HIV-associated sensory neuropathy. Patients were randomly assigned to smoke either cannabis (3.56% tetrahydrocannabinol) or identical placebo cigarettes with the cannabinoids extracted three times daily for 5 days. Primary outcome measures included ratings of chronic pain and the percentage achieving >30% reduction in pain intensity. Acute analgesic and anti-hyperalgesic effects of smoked cannabis were assessed using a cutaneous heat stimulation procedure and the heat/capsaicin sensitization model.
Results: Fifty patients completed the entire trial. Smoked cannabis reduced daily pain by 34% (median reduction; IQR = −71, −16) vs 17% (IQR = −29, 8) with placebo (p = 0.03). Greater than 30% reduction in pain was reported by 52% in the cannabis group and by 24% in the placebo group (p = 0.04). The first cannabis cigarette reduced chronic pain by a median of 72% vs 15% with placebo (p < 0.001). Cannabis reduced experimentally induced hyperalgesia to both brush and von Frey hair stimuli (p ≤ 0.05) but appeared to have little effect on the painfulness of noxious heat stimulation. No serious adverse events were reported.
Conclusion: Smoked cannabis was well tolerated and effectively relieved chronic neuropathic pain from HIV-associated sensory neuropathy. The findings are comparable to oral drugs used for chronic neuropathic pain.

Get full access to this article

View all available purchase options and get full access to this article.

References

1.
So YT, Holtzman DM, Abrams DI, Olney RK. Peripheral neuropathy associated with acquired immunodeficiency syndrome. Arch Neurol 1988;45:945–948.
2.
Sacktor N. The epidemiology of human immunodeficiency virus-associated neurological disease in the era of highly active retroviral therapy. J Neurovirol 2002;8(suppl 2):115–121.
3.
McArthur JC, Brew BJ, Nath A. Neurological complications of HIV infection. Lancet Neurol 2005;4:543–555.
4.
Simpson DM, McArthur JC, Olney R, et al. Lamotrigine for HIV-associated painful sensory neuropathies: a placebo-controlled trial. Neurology 2003;60:1508–1514.
5.
Hahn K, Arendt G, Braun JS. A placebo-controlled trial of gabapentin for painful HIV-associated sensory neuropathies. J Neurol 2004;251:1260–1266.
6.
Hugen PW, Burger DM, Brinkman K, et al. Carbamazepine-indinavir interaction causes antiretroviral therapy failure. Ann Pharmacother 2000;34:465–470.
7.
Simpson DM, Dorfman D, Olney RK, et al. Peptide T in the treatment of painful distal neuropathy associated with AIDS: results of a placebo-controlled trial. Neurology 1996;47:1254–1259.
8.
Kemper CA, Kent G, Burton S, Deresinski SC. Mexiletine for HIV-infected patients with painful peripheral neuropathy: a double-blind, placebo-controlled, crossover treatment trial. J Acquir Immune Defic Syndr Hum Retrovirol 1998;19:367–372.
9.
Keiburtz K, Simpson D, Yiannoutsos C, et al. A randomized trial of amitriptyline and mexiletine for painful neuropathy in HIV infection. Neurology 1998;51:1682–1688.
10.
Shlay JC, Chaloner K, Max MG, et al. Acupuncture and amitriptyline for pain due to HIV-related peripheral neuropathy: a randomized clinical trial. JAMA 1998;280:1590–1595.
11.
Paice JA, Ferrans CE, Lashley FR, Shott S, Vizgirda V, Pitrak D. Topical capsaicin in the management of HIV-associated peripheral neuropathy. J Pain Symptom Manage 2000;19:45–52.
12.
Calignano A, LaRana G, Giuffrida A, Piomelli D. Control of pain initiation by endogenous cannabinoids. Nature 1998;394:277–281.
13.
Walker JM, Huang SM. Cannabinoid analgesia. Pharmacol Ther 2002;95:127–135.
14.
Petersen KL, Maloney A, Hoke F, Dahl JB, Rowbotham MC. A randomized study of the effect of oral lamotrigine and hydromorphone on pain and hyperalgesia following heat/capsaicin sensitization. J Pain 2003;4:400–406.
15.
Petersen KL, Rowbotham MC. A new human experimental pain model: the heat/capsaicin sensitization model. Neuroreport 1999;10:1511–1516.
16.
Foltin RW, Fischman MW, Byrne MF. Effects of smoked cannabis on food intake and body weight of humans living in a residential laboratory. Appetite 1988;25:577–582.
17.
Petersen KL, Jones B, Segredo V, Dahl JB, Rowbotham MC. Effect of remifentanil on pain and secondary hyperalgesia associated with the heat-capsaicin sensitization model in healthy volunteers. Anesthesiology 2001;94:15–20.
18.
Dirks J, Petersen KL, Rowbotham MC, Dahl JB. Gabapentin suppresses cutaneous hyperalgesia following heat/capsaicin sensitization. Anesthesiology 2002;97:102–107.
19.
Dirks K, Petersen KL, Dahl JB. The heat capsaicin sensitization model: a methodological study. J Pain 2003;4:122–128.
20.
McNair DM, Lorr M, Droppleman LF. Manual for the Profile of Mood States (POMS). San Diego: Educational and Industrial Testing Service, 1971.
21.
NIH Division of AIDS Table for Grading Severity of Adult Adverse Experiences, August 1992. Available at: http://rcc.tech-res-intl.com/tox_tables.htm. Accessed March 6, 2006.
22.
Jay C, Shade S, Vizoso H, et al. The effect of smoked cannabis on chronic neuropathic and experimentally-induced pain in HIV neuropathy: results of an open-label pilot study. 11th Conference on Retroviruses and Opportunistic Infections 2004: abstract 496:243.
23.
Farrar JT, Young JP Jr, LaMoreaux L, Werth JL, Poole RM. Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale. Pain 2001;94:149–158.
24.
Finnerup NB, Otto M, McQuay HJ, Jensen TS, Sindrup SH. Algorithm for neuropathic pain treatment: an evidence based proposal. Pain 2005;118:289–305.
25.
Rowbotham M, Harden N, Stacey B, Bernstein P, Magnus-Miller L. Gabapentin for the treatment of postherpetic neuralgia: a randomized controlled trial. JAMA 1998;280:1837–1842.
26.
Backonja M, Beydoun A, Edwards KR, et al. Gabapentin for the symptomatic treatment of painful neuropathy in patients with diabetes mellitus: a randomized controlled trial. JAMA 1998;280:1831–1836.
27.
Rowbotham MC, Twilling L, Davies PS, Reisner L, Taylor K, Mohr D. Oral opioid therapy for chronic peripheral and central neuropathic pain. N Engl J Med 2003;348:1223–1232.
28.
Eisenberg E, McNichol ED, Carr DB. Efficacy and safety of opioid agonists in the treatment of neuropathic pain of nonmalignant origin: Systematic review and meta-analysis of randomized controlled trials. JAMA 2005;293:3043–3052.
29.
Grunfeld Y, Edery H. Psychopharmacological activity of the active constituents of hashish and some related cannabinoids. Psychopharmacologia 1969;14:200–210.
30.
Buxbaum DM. Analgesic activity of 9 -tetrahydrocannabinol in the rat and mouse. Psychopharmacologia 1972;25:275–280.
31.
Chesher GB, Dahl CJ, Everingham M, Jackson DM, Marchant-Williams H, Starmer GA. The effect of cannabinoids on intestinal motility and their antinociceptive effect in mice. Br J Pharmacol 1973;49:588–594.
32.
Sofia RD, Vassar HB, Nalepa SD. Correlations between pathological changes in the hind paws of rats with adjuvant arthritis and their response to anti-inflammatory and analgesic drugs. Eur J Pharmacol 1973;24:108–112.
33.
Moss DE, Johnson RL. Tonic analgesic effects of delta 9-tetrahydrocannabinol as measured with the formalin test. Eur J Pharmacol 1980;61:313–315.
34.
Li J, Daughters RS, Bullis C, et al. The cannabinoid receptor agonist WIN 55,212-2 mesylate blocks the development of hyperalgesia produced by capsaicin in rats. Pain 1999;81:25–33.
35.
Herzberg U, Eliav E, Bennett GJ, Kopin IJ. The analgesic effect of R(+)-WIN 55,212-2 mesylate, a high affinity cannabinoid agonist, in a rat model of neuropathic pain. Neurosci Lett 1997;221:157–160.
36.
Milstein SL, MacCannell K, Karr G, Clark S. Cannabis-produced changes in pain tolerance. Experienced and non-experienced subjects. Int Pharmacopsychiatry 1975;10:177–182.
37.
Noyes R Jr, Baram DA. Cannabis analgesia. Compr Psychiatry 1974;15:531–535.
38.
Noyes R, Brunk S, Avery D, Canter A. The analgesic properties of delta-9-tertrahydrocannabinol and codeine. Clin Pharmacol Ther 1975;18:84–89.
39.
Svendsen KB, Jensen TS, Back FW. Does the cannabinoid dronabinol reduce central pain in multiple sclerosis? Randomised double blind placebo controlled crossover trial. BMJ 2004;329:253–260.
40.
Rog DJ, Nurmikko TJ, Fride T, Young CA. Randomized, controlled trial of cannabis-based medicine in central pain in multiple sclerosis. Neurology 2005;65:812–819.
41.
Joy J, Watson S, Bensen J. Cannabis and medicine: assessing the science base. Washington, DC: National Academy Press; 1999. Available at: http://www.nap.edu
42.
Attal N, Brasseur L, Guirimand D, Clermond-Gnamien S, Atlamis S, Bouhassira D. Are oral cannabinoids safe and effective in refractory neuropathic pain? Eur J Pain 2004;8:173–177.
43.
Woolridge E, Barton S, Samuel J, Osorio J, Dougherty A, Holdcroft A. Cannabis use in HIV for pain and other medical symptoms. J Pain Symptom Manage 2005;29:358–367.
44.
Abrams DI, Hilton JF, Leiser RJ, et al. Short-term effects of cannabinoids in patients with HIV-1 infection: a randomized, placebo-controlled clinical trial Ann Intern Med 2003;139:258–299.

Information & Authors

Information

Published In

Neurology®
Volume 68Number 7February 13, 2007
Pages: 515-521
PubMed: 17296917

Publication History

Published online: February 12, 2007
Published in print: February 13, 2007

Permissions

Request permissions for this article.

Authors

Affiliations & Disclosures

D. I. Abrams, MD
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.
C. A. Jay, MD
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.
S. B. Shade, MPH
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.
H. Vizoso, RN
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.
H. Reda, BA
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.
S. Press, BS
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.
M. E. Kelly, MPH
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.
M. C. Rowbotham, MD
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.
K. L. Petersen, MD
From the Community Consortium, Positive Health Program (D.I.A., S.B.S., H.V., M.E.K.), Hematology-Oncology (D.I.A., M.E.K.), and Neurology (C.A.J.), Divisions at San Francisco General Hospital; and Departments of Medicine (D.I.A., S.B.S., H.V., M.E.K.) and Neurology (C.A.J., H.R., S.P., M.C.R., K.L.P.), and the UCSF Pain Clinical Research Center (H.R., S.P., M.C.R., K.L.P.), University of California San Francisco.

Notes

Address correspondence and reprint requests to Dr. Donald I. Abrams, San Francisco General Hospital, Ward 84, 995 Potrero Avenue, San Francisco, CA 94110; e-mail: [email protected]

Metrics & Citations

Metrics

Citation information is sourced from Crossref Cited-by service.

Citations

Download Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Select your manager software from the list below and click Download.

Cited By
  1. Cannabis Compounds: Potential Therapy for Neurological Disease, Medicinal Plants - Harnessing the Healing Power of Plants, (2024).https://doi.org/10.5772/intechopen.1005770
    Crossref
  2. Cannabis Use and Cannabidiol Modulate HIV-Induced Alterations in TREM2 Expression: Implications for Age-Related Neuropathogenesis, Viruses, 16, 10, (1509), (2024).https://doi.org/10.3390/v16101509
    Crossref
  3. CBD and THC in Special Populations: Pharmacokinetics and Drug–Drug Interactions, Pharmaceutics, 16, 4, (484), (2024).https://doi.org/10.3390/pharmaceutics16040484
    Crossref
  4. Research and Clinical Practice Involving the Use of Cannabis Products, with Emphasis on Cannabidiol: A Narrative Review, Pharmaceuticals, 17, 12, (1644), (2024).https://doi.org/10.3390/ph17121644
    Crossref
  5. Feasibility of a Randomized, Interventional Pilot Clinical Study of Oral Cannabinoids in People with HIV on Antiretroviral Therapy: CTNPT 028, Journal of Personalized Medicine, 14, 7, (745), (2024).https://doi.org/10.3390/jpm14070745
    Crossref
  6. Cannabinoid Analgesia in Postoperative Pain Management: From Molecular Mechanisms to Clinical Reality, International Journal of Molecular Sciences, 25, 11, (6268), (2024).https://doi.org/10.3390/ijms25116268
    Crossref
  7. The Efficacy of Cannabis in Oncology Patient Care and Its Anti-Tumor Effects, Cancers, 16, 16, (2909), (2024).https://doi.org/10.3390/cancers16162909
    Crossref
  8. Effects of acute cannabidiol on behavior and the endocannabinoid system in HIV-1 Tat transgenic female and male mice, Frontiers in Neuroscience, 18, (2024).https://doi.org/10.3389/fnins.2024.1358555
    Crossref
  9. Medicinal Plants for the Treatment of Neuropathic Pain: A Review of Randomized Controlled Trials, Current Pharmaceutical Biotechnology, 25, 5, (534-562), (2024).https://doi.org/10.2174/1389201024666230714143538
    Crossref
  10. Nanocarriers for Cannabinoid Delivery: Enhancing Therapeutic Potential, Recent Advances in Drug Delivery and Formulation, 18, 4, (247-261), (2024).https://doi.org/10.2174/0126673878300347240718100814
    Crossref
  11. See more
Loading...

View Options

Login options

Check if you have access through your login credentials or your institution to get full access on this article.

Personal login Institutional Login
Purchase Options

The neurology.org payment platform is currently offline. Our technical team is working as quickly as possible to restore service.

If you need immediate support or to place an order, please call or email customer service:

  • 1-800-638-3030 for U.S. customers - 8:30 - 7 pm ET (M-F)
  • 1-301-223-2300 for customers outside the U.S. - 8:30 - 7 pm ET (M-F)
  • [email protected]

We appreciate your patience during this time and apologize for any inconvenience.

View options

PDF and All Supplements

Download PDF and Supplementary Material

Full Text

View Full Text

Full Text HTML

View Full Text HTML

Figures

Tables

Media

Share

Share

Share article link

Share