Cited by 58Cannabis and Cannabinoid ResearchPain Mechanisms and TreatmentsPain Management and Opioid Use

Pain measurements and side effect profile of the novel cannabinoid ajulemic acid

Salim, Kahlid, Schneider, Udo, Burstein, Sumner, Hoy, Ludwig, Karst, Matthias·2005·Neuropharmacology

Abstract

Preclinical findings on ajulemic acid (AJA) showed analgesic and anti-allodynic effects without psychoactive properties making it an appealing substance for the treatment of pain. A recently published randomized double-blind crossover clinical trial described the pain-reducing effects and side effect profile of AJA on 21 patients with chronic neuropathic pain. In this report from this same sample the effects of AJA on the mechanical hypersensitivity, on pain, and on psychological and physical performance were further characterized. During a 5-week study period, patients were divided into two 7-day treatment groups receiving either AJA or placebo capsules first, respectively. All patients received 40 and 80 mg of AJA or placebo daily in each treatment period. Pain measurements included the determination of mechanical hypersensitivity using the von Frey hair method as well as the visual analog scale (VAS), for which the number needed to treat (NNT) was calculated. The side effect profile of the compound was evaluated using psychotropic and physical measurements as well as obtaining reports on possible subjective side effects. The results showed no significant reduction in mechanical hypersensitivity (p=0.052), although a tendency towards pain reduction could be seen. The VAS score showed significant pain reduction (p=0.021) and NNT values for 30% pain relief were 2.14 for the first treatment group and 5.29 for the second treatment group. No significant findings were observed regarding psychotropic or physical measurements. Reported subjective side effects were mainly dry mouth, tiredness and dizziness and did not increase with dose elevation. Overall, these study findings indicate that AJA shows pain-reducing effects on patients with chronic neuropathic pain without clinically relevant psychotropic or physical side effects.

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Crossref · 10.1016/j.neuropharm.2005.02.010

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  • Patients showed a trend towards decreased mechanical allodynia following CT-3 administration.

    “Eighteen of those same patients participated in stimulus-evoked pain testing during the study and patients showed a trend towards decreased mechanical allodynia following CT-3 administration.153”

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References 28 · Cited by 58

Authors
Salim, K., Schneider, U., Burstein, S., Hoy, L., & Karst, M.
Affiliations
  • Medizinische Hochschule Hannover (DE)
  • University of Massachusetts Chan Medical School (US)
Corresponding author
Karst, Matthias
Venue
Neuropharmacology
Publisher
Elsevier BV
Published
2005-06
Volume
48
Issue
8
Pages
1164-1171
ISSN
0028-3908 (ISSN-L)
OpenAlex
W2117626900
Cited by
58
References
28
Citations by year
2024: 1 · 2023: 1 · 2021: 1 · 2020: 4 · 2019: 2 · 2018: 3 · 2017: 1 · 2016: 2 · 2015: 2 · 2014: 4 · 2013: 1 · 2012: 7
FWCI
4.04
Type
journal article
Language
en
Open access
closed
Locations
  • Neuropharmacology (publishedVersion)
  • PubMed (publishedVersion)
Funders
Medizinischen Hochschule Hannover
Topics
  • Health Sciences › Medicine › Pharmacology › Cannabis and Cannabinoid Research
  • Health Sciences › Medicine › Physiology › Pain Mechanisms and Treatments
  • Health Sciences › Medicine › Anesthesiology and Pain Medicine › Pain Management and Opioid Use
Keywords
ajulemic acid, chronic neuropathic pain, mechanical hypersensitivity, number needed to treat, adverse effects, xerostomia, dizziness, fatigue, psychoactive effects
MeSH terms
Adult, Aged, Female, Humans, Hyperalgesia, Male, Middle Aged, Pain Measurement, Dronabinol, Touch, Cross-Over Studies

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