Pilot RCT comparing low-dose naltrexone, gabapentin and placebo to reduce pain among people with HIV with alcohol problems

PLoS One. 2024 Feb 26;19(2):e0297948. doi: 10.1371/journal.pone.0297948. eCollection 2024.

Abstract

Background: To estimate the effects on pain of two medications (low-dose naltrexone and gabapentin) compared to placebo among people with HIV (PWH) with heavy alcohol use and chronic pain.

Methods: We conducted a pilot, randomized, double-blinded, 3-arm study of PWH with chronic pain and past-year heavy alcohol use in 2021. Participants were recruited in St. Petersburg, Russia, and randomized to receive daily low-dose naltrexone (4.5mg), gabapentin (up to 1800mg), or placebo. The two primary outcomes were change in self-reported pain severity and pain interference measured with the Brief Pain Inventory from baseline to 8 weeks.

Results: Participants (N = 45, 15 in each arm) had the following baseline characteristics: 64% male; age 41 years (SD±7); mean 2 (SD±4) heavy drinking days in the past month and mean pain severity and interference were 3.2 (SD±1) and 3.0 (SD±2), respectively. Pain severity decreased for all three arms. Mean differences in change in pain severity for gabapentin vs. placebo, and naltrexone vs. placebo were -0.27 (95% confidence interval [CI] -1.76, 1.23; p = 0.73) and 0.88 (95% CI -0.7, 2.46; p = 0.55), respectively. Pain interference decreased for all three arms. Mean differences in change in pain interference for gabapentin vs. placebo, and naltrexone vs. placebo was 0.16 (95% CI -1.38, 1.71; p = 0.83) and 0.40 (95% CI -1.18, 1.99; p = 0.83), respectively.

Conclusion: Neither gabapentin nor low-dose naltrexone appeared to improve pain more than placebo among PWH with chronic pain and past-year heavy alcohol use.

Clinical trial registration: ClinicalTrials.gov (NCT4052139).

Trial registration: ClinicalTrials.gov NCT04052139.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Alcohol-Related Disorders*
  • Chronic Pain* / complications
  • Chronic Pain* / drug therapy
  • Double-Blind Method
  • Female
  • Gabapentin / therapeutic use
  • HIV Infections* / complications
  • HIV Infections* / drug therapy
  • Humans
  • Male
  • Middle Aged
  • Naltrexone / therapeutic use
  • Pain Management
  • Treatment Outcome

Substances

  • Gabapentin
  • Naltrexone

Associated data

  • ClinicalTrials.gov/NCT04052139

Grants and funding

This work was supported by the National Institutes of Health (UH3AA026193 [JHS, JIT], UH2AA026193 [JHS, JIT], U24AA020778 [JHS], U24AA020779 [DMC], P30AI042853, P30AI027757). The sponsor websites are the following: https://www.niaaa.nih.gov/ and https://www.niaid.nih.gov/. Dr. Kendall Bryant, an employee of NIAAA, is a co-author on the manuscript. Dr. Misha Backonja, a current employee of NICCH, is a co-author on the manuscript, but was not an employee of NIH when the study was conducted. Otherwise, the funding source had no role in study design, the collection, analysis and interpretation of data, in the writing of the report or in the decision to submit the article for publication. The specific roles of these authors are articulated in the ‘author contributions’ section. The content is solely the responsibility of the authors and does not represent the official views of the National Institutes of Health. There was no additional external funding received for this study.