Study register · detail
Clear benefit
GRADE
Low
253 citations
Samplen = 30 Pat.
DurationPhase I
ControlPlacebo capsules
EndpointPain intensity
Blindingdoppelblind
DesignRCT
Cannabinoidthc
Max. dose20.0 mg
Routeoral
Key finding
Dronabinol led to decreased pain intensity, increased patient satisfaction, and significant pain relief as adjuvant therapy in opioid-treated chronic pain patients.
Summary
n=30 chronic pain patients under opioid therapy, dronabinol 10–20 mg/d adjuvant vs. placebo; no significant difference in the primary endpoint (BPI pain intensity p=0.59), trend towards improved sleep quality.
P
PopulationAdults with chronic non-cancer pain under stable opioid therapy, n=30
I
InterventionDronabinol (synthetic Δ9-THC) 10 mg or 20 mg orally, Phase I: single-dose crossover; Phase II: open-label titrated as add-on
C
ControlPlacebo capsules (Phase I randomised, double-blind, crossover)
O
OutcomePhase I: significant reduction in pain intensity and increased patient satisfaction vs. placebo, no difference 10 mg vs. 20 mg; Phase II: significant pain relief vs. baseline
Confidence in the evidence
Low
The second of four GRADE levels, the effect estimate is of limited reliability.
Downgraded for
Risk of biasImprecision
Quality profile
Sample size
★★★★★
Blinding
Double-blind
Effect size
Clear benefit
Citations / year
★★★★★
Authors
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Abstract
Perspective: This study examines the effect of adding a cannabinoid to the regimen of patients with chronic pain who report significant pain despite taking stable doses of opioids. The results of our preliminary study suggest that dronabinol, a synthetic THC, may have an additive effect on pain relief.
The impediment to action advances action.