Schlafstörungen
Studienlage · Detail RCT · Schlafstörungen · 2026

Cannabinol for Acute Treatment of Insomnia Disorder in a Randomized Placebo-Controlled Crossover Trial.

Keine Richtungsangabe GRADE Moderat
Stichproben = 20 Pat.
DesignRCT
Zusammenfassung

n=20 Erwachsene mit Insomnie-Diagnose (DSM-5/ICSD-3, ISI≥15), randomisierte placebo-kontrollierte Cross-over-Studie zu Cannabinol (CBN) 30 mg vs. 300 mg vs. Placebo. Primärer Endpunkt WASO (Wake After Sleep Onset) ohne signifikante Reduktion (300 mg: -6,3 min [95% CI: -18,2 bis +5,5], p=0,29, dz=-0,22; 30 mg: -4,0 min [-15,9 bis +7,9], p=0,50, dz=0,11). Sekundäre Outcomes bei 300 mg CBN: Zunahme NREM-2-Schlaf (p=0,03, dz=0,54), verbesserte subjektive Schlafqualität (p=0,005, dz=0,56), Reduktion der Einschlaflatenz (p=0,004, dz=-0,74) und EEG-Arousal-Indizes (p=0,02, dz=-0,65). Insgesamt 247 leichte bis moderate Nebenwirkungen über alle Arme.

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Moderat

Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.

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Autoren
Lavender IG, Marshall NS, McCartney D, Cho G, Irwin C, Suraev A, Gordon R, Arnold JC, D'Rozario AL, Gordon CJ
DOI 10.1111/jsr.70284
Design: RCT
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Abstract
Insomnia disorder is harmful and requires novel treatments. Cannabinol, an oxidative by-product of Delta9-tetrahydrocannabinol, is claimed to be a hypnotic, but its effects on objective sleep and insomnia remain unknown. This randomized, double-blind, placebo-controlled, three-arm, single-night crossover trial evaluated the acute efficacy and safety of cannabinol for insomnia disorder. Twenty adults (aged 25-65) with physician-diagnosed insomnia disorder (meeting DSM-5 and ICSD-3 criteria; Insomnia Severity Index >/= 15) were enrolled at the Woolcock Institute of Medical Research (Sydney, Australia) between August 2022 and September 2023. Participants received a single 2 mL oral dose of 30 mg (1.5%) or 300 mg (15%) cannabinol, or matched placebo (2-week washout). All participants (17 female and 3 males; mean +/- SD age 42 +/- 13 years) completed the protocol and were statistically analysed. The primary outcome was wake after sleep onset (WASO) minutes, measured by overnight polysomnography. Cannabinol did not significantly change WASO (300 mg: -6.3 min [95% CI: -18.2, +5.5], p = 0.29, dz = -0.22; 30 mg: -4.0 min [-15.9, +7.9], p = 0.50, dz = 0.11). However, 300 mg cannabinol increased non-rapid eye movement-2 sleep (p = 0.03, dz = 0.54), subjective sleep quality (p = 0.005, dz = 0.56); and reduced sleep onset latency (p = 0.004, dz = -0.74) and electroencephalographic arousal indices (p = 0.02, dz = -0.65). There were 247 mild-to-moderate adverse events across arms. Larger, longer trials are warranted. ClinicalTrials.gov Identifier: NCT05344170.

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