Safety of Co-Administered Cannabidiol (CBD) and alcohol: a Phase I study.

IF 3.8 Q1 PHARMACOLOGY & PHARMACY
David Wolinsky, Sara Blaine, Justin C Strickland, Erica N Peters, Amy Harrison, Elise M Weerts, Marcel O Bonn-Miller
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引用次数: 0

Abstract

Background: This Phase I randomized controlled trial aimed to assess the safety and tolerability of cannabidiol (CBD) and alcohol co-administration among moderate alcohol consumers in acute laboratory and chronic outpatient settings.

Methods: Healthy adults ages 21-65 with moderate alcohol use completed three acute dosing sessions where they received either placebo, 50 mg CBD, or 100 mg CBD along with alcohol dosed to achieve peak blood alcohol concentrations (BAC) of 0.06 g/100 mL. Sessions were randomly ordered, and participants and outcome assessors were blinded to study drug during these laboratory sessions. Breath alcohol content (BrAC) and measures of subjective effects and impairment were collected from participants throughout each session. Participants then consumed 50 mg CBD twice daily for four weeks as outpatients while reporting alcohol use, craving, and adverse effects via a smartphone app. Metabolic labs and CBD content were measured from blood samples collected at four-week follow-up.

Results: Twenty-nine participants were enrolled and nineteen participants completed the study. CBD was well-tolerated in both acute and chronic dosing sessions. Acute CBD-alcohol use was not associated with significant differences in subjective responses or breath alcohol content (BrAC) peak or time course compared to placebo for either CBD condition. Acute CBD-alcohol use was not associated with impairment 4 h after dosing. CBD use was not associated with significant changes in alcohol cravings or drinks per day, nor significant lab changes outside of decreases in protein and globulin, across the chronic dosing period.

Conclusions: CBD co-administration with alcohol was not associated with significant changes in subjective or physiologic effects among moderate alcohol consumers in acute laboratory and naturalistic outpatient settings. The safety of CBD use in patients with more severe alcohol use should be examined in future studies.

Trial registration: This study was registered at ClinicalTrials.gov on April 7th, 2022 under the code NCT05317507 .

大麻二酚(CBD)和酒精联合使用的安全性:一项I期研究
背景:本I期随机对照试验旨在评估急性实验室和慢性门诊中度酒精消费者中大麻二酚(CBD)和酒精联合给药的安全性和耐受性。方法:年龄21-65岁、适度饮酒的健康成年人完成了三个急性给药阶段,其中他们接受安慰剂、50 mg CBD或100 mg CBD以及酒精剂量,以达到血液酒精浓度(BAC)峰值0.06 g/100 mL。实验阶段随机排序,参与者和结果评估者在这些实验室阶段采用盲法研究药物。呼气酒精含量(BrAC)以及主观影响和损害的测量在每个疗程中收集。然后,作为门诊病人,参与者每天两次摄入50毫克CBD,持续四周,同时通过智能手机应用程序报告酒精使用、渴望和不良反应。在四周的随访中,从收集的血液样本中测量代谢实验室和CBD含量。结果:29名参与者入组,19名参与者完成了研究。CBD在急性和慢性给药过程中都具有良好的耐受性。与安慰剂相比,急性CBD酒精使用与主观反应或呼吸酒精含量(BrAC)峰值或时间过程的显着差异无关。急性cbd酒精使用与给药后4小时的损伤无关。在整个慢性给药期间,CBD的使用与每天对酒精的渴望或饮酒的显著变化无关,除了蛋白质和球蛋白的减少之外,也没有显著的实验室变化。结论:在急性实验室和自然门诊环境中,CBD与酒精联合给药与中度酒精消费者的主观或生理效应的显著变化无关。在未来的研究中,应该对重度饮酒患者使用CBD的安全性进行检查。试验注册:本研究于2022年4月7日在ClinicalTrials.gov注册,代码为NCT05317507。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.20
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