Updated Review: Does Cannabis Actually Help Chronic Pain?

THC-containing products may slightly reduce chronic pain — but the benefit is small and comes with significant side effects like dizziness, sedation, and nausea.

Chou, Roger et al.·Annals of internal medicine·2026·Moderate EvidenceSystematic Review·1 min read
RTHC-08168Systematic ReviewModerate Evidence2026RETHINKTHC RESEARCH DATABASErethinkthc.com/research

Quick Facts

Study Type
Systematic Review
Evidence
Moderate Evidence
Sample
N=2,303
Participants
25 randomized controlled trials (N=2,303; 64% with neuropathic pain).

What This Study Found

This updated systematic review pooled data from 25 randomized controlled trials involving 2,303 patients, most with neuropathic pain. The findings split sharply by cannabinoid type and formulation.

Oral synthetic or purified THC-only products (like dronabinol and nabilone) showed mixed results: nabilone moderately reduced pain severity (by about 1.6 points on a 10-point scale), but dronabinol showed essentially no benefit (only 0.23 points). Oromucosal sprays with comparable THC-to-CBD ratios (like nabiximols/Sativex) probably slightly reduced pain, by about half a point.

Products with low THC-to-CBD ratios — including CBD-dominant formulations — did not improve pain outcomes in the trials analyzed.

Across nearly all THC-containing products, participants experienced substantially more dizziness, sedation, and nausea compared to placebo. The pattern was consistent: modest pain relief came paired with a meaningful side effect burden.

Key Numbers

25 RCTs, 2,303 patients, 64% with neuropathic pain. Pain reduction on 0–10 scale: nabilone −1.59 points, oromucosal comparable THC:CBD −0.54 points, dronabinol −0.23 points (not significant). Low THC:CBD products showed no improvement. Significant increases in dizziness, sedation, and nausea across THC-containing products.

How They Did This

Systematic review searching Ovid MEDLINE, PsycINFO, Embase, Cochrane Library, and Scopus through July 2025. Included only randomized placebo-controlled trials of cannabinoids for chronic pain lasting 1–6 months. Cannabinoids were categorized by THC-to-CBD ratio, source (synthetic, purified, extracted), and administration method. Risk of bias and strength of evidence were independently reviewed by two assessors.

Why This Research Matters

Cannabis is increasingly used and recommended for chronic pain, but the evidence base has been unclear. This review — published in the Annals of Internal Medicine, one of the most selective medical journals — provides the most current synthesis available and draws a clearer line between which cannabinoid types show benefit and which do not.

The Bigger Picture

This review reinforces a growing pattern in cannabinoid research: the type of cannabinoid product matters enormously. Nabilone (a synthetic THC analog) outperformed plant-derived THC, while CBD-dominant products showed no pain benefit in controlled trials. For the millions of people using cannabis products for pain based on anecdotal evidence, the clinical trial data tell a more nuanced story — one where specific formulations matter and side effects are part of the equation. This connects to the broader Cochrane neuropathic pain review (RTHC-00225) which reached similar conclusions about modest benefit and significant harms.

What This Study Doesn't Tell Us

Most trials were short-term (1–6 months), so long-term efficacy and safety remain unknown. The 64% neuropathic pain concentration means results may not generalize well to other chronic pain types. Many trials had moderate risk of bias. Cannabis product formulations varied across studies, making direct comparisons imperfect.

Questions This Raises

  • ?Why does nabilone outperform dronabinol despite both being THC-type compounds?
  • ?Would longer-term trials show tolerance development that erodes the modest benefits seen at 1–6 months?
  • ?Are there chronic pain subtypes where cannabinoids might show larger effects?

Trust & Context

Key Stat:
Evidence Grade:
Systematic review of 25 randomized controlled trials published in a top-tier journal — this represents some of the strongest evidence available on cannabinoids for pain, though individual trial quality varied.
Study Age:
Published in 2026 with literature search through July 2025, making this the most current systematic review on cannabinoids for chronic pain.
Original Title:
Cannabis-Based Products for Chronic Pain : An Updated Systematic Review.
Published In:
Annals of internal medicine, 179(2), 230-241 (2026)The Annals of Internal Medicine is a well-respected journal known for publishing high-quality clinical research.
Funding:
Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services.
Database ID:
RTHC-08168

Evidence Hierarchy

Meta-Analysis / Systematic ReviewCombines many studies into one answer
This study
Randomized Controlled Trial
Cohort / Case-Control
Cross-Sectional / Observational
Case Report / Animal Study

Analyzes all available research on a topic using a structured method.

What do these levels mean? →

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Cite This Study

RTHC-08168·https://rethinkthc.com/research/RTHC-08168

APA

Chou, Roger; Fu, Rongwei; Ahmed, Azrah Y; Morasco, Benjamin J. (2026). Cannabis-Based Products for Chronic Pain : An Updated Systematic Review.. Annals of internal medicine, 179(2), 230-241. https://doi.org/10.7326/ANNALS-25-03152

MLA

Chou, Roger, et al. "Cannabis-Based Products for Chronic Pain : An Updated Systematic Review.." Annals of internal medicine, 2026. https://doi.org/10.7326/ANNALS-25-03152

RethinkTHC

RethinkTHC Research Database. "Cannabis-Based Products for Chronic Pain : An Updated System..." RTHC-08168. Retrieved from https://rethinkthc.com/research/chou-2026-cannabisbased-products-for-chronic

Access the Original Study

Study data sourced from PubMed, a service of the U.S. National Library of Medicine, National Institutes of Health.

This study breakdown was produced by the RethinkTHC research team. We analyze and report published research findings without making health recommendations. All interpretations are based solely on the published abstract and study data.