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Study register · detail RCT (cross-over, gesunde Probanden) · Psychosis Risk · 2012

Acute Effects of a Single, Oral dose of d9-tetrahydrocannabinol (THC) and Cannabidiol (CBD) Administration in Healthy Volunteers

Mixed GRADE Moderate 288 citations
Samplen = 16 Pat.
Duration3 sessions at one-month…
ControlPlacebo
EndpointSymptom scaling
Blindingdoppelblind
DesignRCT (cross-over, gesunde Probanden)
Cannabinoidkombination
Max. dose600.0 mg
Routeoral
Key finding

THC induced pronounced acute psychological and physiological effects, CBD was indistinguishable from placebo.

Summary

Randomised double-blind cross-over trial n=16 healthy male subjects; oral THC 10 mg vs. CBD 600 mg vs. placebo; THC vs. placebo: significant positive psychotic symptoms, anxiety, dysphoria (AUC and effect at 2h: p<0,01); CBD: no significant differences from placebo on psychotic or anxiety symptoms — CBD safety signal with regard to psychosis.

P
PopulationHealthy male subjects, n=16
I
InterventionOral THC 10 mg or oral CBD 600 mg, single dose, cross-over
C
ControlPlacebo (oral)
O
OutcomeTHC vs. placebo/CBD: significantly more anxiety, dysphoria, psychotic symptoms, sedation, subjective intoxication (AUC and 2h effect p<0,01) as well as increased heart rate (p<0,05); no differences between CBD and placebo
Confidence in the evidence
Moderate

The third of four GRADE levels, the effect estimate is probably reliable.

Downgraded for
Imprecision
Quality profile
Sample size ★★★★★
Blinding Double-blind
Effect size Mixed
Citations / year ★★★★★
Authors
Martin-Santos R, A. Crippa J, Batalla A et al.
DOI 10.2174/138161212802884780↗
Design: RCT (cross-over, gesunde Probanden)
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Abstract
<h4>Rationale</h4>Animal and humans studies suggest that the two main constituents of cannabis sativa, delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) have quite different acute effects. However, to date the two compounds have largely been studied separately.<h4>Objective</h4>To evaluate and compare the acute pharmacological effects of both THC and CBD in the same human volunteers.<h4>Methods</h4>A randomised, double-blind, cross-over, placebo controlled trial was conducted in 16 healthy male subjects. Oral THC 10 mg or CBD 600 mg or placebo was administered in three consecutive sessions, at one-month interval. Physiological measures and symptom ratings were assessed before, and at 1, 2 and 3 hours post drug administration. The area under the curve (AUC) between baseline and 3 hours, and the maximum absolute change from baseline at 2 hours were analysed by one-way repeated measures analysis of variance, with drug condition (THC or CBD or placebo) as the factor.<h4>Results</h4>Relative to both placebo and CBD, administration of THC was associated with anxiety, dysphoria, positive psychotic symptoms, physical and mental sedation, subjective intoxication (AUC and effect at 2 hours: p < 0.01), an increase in heart rate (p < 0.05). There were no differences between CBD and placebo on any symptomatic, physiological variable.<h4>Conclusions</h4>In healthy volunteers, THC has marked acute behavioural and physiological effects, whereas CBD has proven to be safe and well tolerated.

The impediment to action advances action. — Marcus Aurelius