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临床试验/NCT04605393
NCT04605393已完成不适用

Does Cannabidiol Attenuate the Acute Effects of ∆9-tetrahydrocannabinol Intoxication in Individuals Diagnosed With Schizophrenia? A Double-blind, Randomised, Placebo-controlled Experimental Study

King's College London1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2021年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
36
试验地点
1
主要终点
Hopkins Verbal Learning Test

研究概览

简要总结

This study will recruit schizophrenia patients who use cannabis recreationally. Each participant will attend the laboratory on three occasions: an initial visit to check that they are safe to join the study and two days of testing.

Participants will be administered, in a randomized order, a pre-treatment with either CBD (1000mg) orally or a matching placebo. On both experiments, participants will then inhale cannabis containing THC. The THC administration will follow a standardised inhalation procedure using a medical-grade vaporizer device.

Participants will complete a series of tasks measuring cognition, psychosis, anxiety and other subjective experiences.

The study will be carried out at the NIHR-Wellcome Trust Clinical Research Facility at King's College Hospital.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Placebo/THC

Experimental

Oral placebo followed by inhalation of cannabis containing THC.

干预措施: Placebo (Drug)

Placebo/THC

Experimental

Oral placebo followed by inhalation of cannabis containing THC.

干预措施: Delta-9-THC (Drug)

CBD/THC

Experimental

Oral CBD 1000mg followed by inhalation of cannabis containing THC.

干预措施: Cannabidiol (Drug)

CBD/THC

Experimental

Oral CBD 1000mg followed by inhalation of cannabis containing THC.

干预措施: Delta-9-THC (Drug)

结局指标

主要结局

Hopkins Verbal Learning Test

时间窗: Baseline visit; 20 mins post-THC

Delayed verbal recall

Positive and Negative Syndrome Scale

时间窗: pre-CBD/placebo administration, and from immediately after THC inhalation until the end of study visit (i.e. 2-3 hours post-THC)

Positive Subscale

次要结局

  • White Noise Task(Baseline visit; 50 mins post-THC)
  • Plasma delta-9-tetrahydrocannabinol (THC) concentration(pre-CBD/placebo, 90mins post CBD, and 0mins, 5mins, 15mins, +90mins post-THC)
  • Plasma cannabidiol (CBD) concentration(pre-CBD/placebo, 90mins post CBD, and 0mins, 5mins, 15mins, +90mins post-THC)
  • Plasma 11-COOH-THC concentration(pre-CBD/placebo, 90mins post CBD, and 0mins, 5mins, 15mins, +90mins post-THC)
  • Plasma THC-COOH concentraion(pre-CBD/placebo, 90mins post CBD, and 0mins, 5mins, 15mins, +90mins post-THC)
  • Plasma 6-OH-CBD concentration(pre-CBD/placebo, 90mins post CBD, and 0mins, 5mins, 15mins, +90mins post-THC)
  • State-Trait Anxiety Inventory(pre-CBD/placebo administration, pre-THC and 20mins post-THC)
  • Hopkins Verbal Learning Test(Baseline; 20 mins post-THC)
  • Study drug preference(End of Experiment 2)
  • Advice Taking Task(Baseline visit; 30 mins post-THC)
  • State Social Paranoia Scale(pre-CBD/placebo administration, and at the end of study visit (i.e. 2-3 hours post-THC))
  • Visual analogue scales(pre-CBD/placebo, 90mins post CBD, pre-THC, and +10mins, +45mins, +90mins post-THC inhalation, and at the end of study visit (i.e. 2-3 hours post-THC))
  • Psychotomimetic states inventory(pre-CBD/placebo administration, and at the end of study visit (i.e. 2-3 hours post-THC))
  • Plasma 11-OH-THC concentration(pre-CBD/placebo, 90mins post CBD, and 0mins, 5mins, 15mins, +90mins post-THC)
  • Digit span(Baseline; 25 mins post-THC)
  • Positive and Negative Syndrome Scale(pre-CBD/placebo administration, and from immediately after THC inhalation until the end of study visit (i.e. 2-3 hours post-THC))
  • Plasma anandamide concentration(pre-CBD/placebo, 90mins post CBD, and 0mins, 5mins, 15mins, +90mins post-THC)
  • Plasma 2-arachidonoylglycerol concentration.(pre-CBD/placebo, 90mins post CBD, and 0mins, 5mins, 15mins, +90mins post-THC)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Edward Chesney

Psychiatrist/Clinical Research Fellow/Study Co-ordinator

King's College London

研究点 (1)

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