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临床试验/NCT07417059
NCT07417059招募中不适用

The Influence of Female Sex Hormones on the Subjective and Cognitive Response to Cannabis

Maastricht University1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2025年6月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
21
试验地点
1
主要终点
Subjective drug effects

研究概览

简要总结

The goal of this study is to systematically determine whether the cannabis response in human females is related to SH fluctuations throughout the menstrual cycle.

详细描述

Cannabis consumption is increasing globally due to legalization and therapeutic use, prompting concerns about its impact on daily functioning and long-term effects. While research has explored cannabis' risks, the heightened vulnerability of females to its adverse effects has been overlooked. Women experience stronger acute negative reactions and progress to cannabis use disorder faster than men. This gender disparity is likely due to sex hormone (SH) fluctuations related to menstrual cycles, emphasizing the need to study cannabis' differential impact on females to address gender-specific risks and inform treatment approaches. Acute influences of cannabis (300 μg THC/kg bodyweight) on subjective state and cognition will be assessed at three different stages of the menstrual cycle, and compared to a placebo condition in a double-blind, randomized, within-subject study in occasional cannabis using biological females.

Primary Objective: To assess the acute subjective drug effects (good/bad drug effect, drug liking/wanting, anxiety), cognition (attention, working memory, information processing speed, verbal memory, verbal fluency, motor inhibition), and pharmacokinetics of cannabis in females across 3 different phases of the menstrual cycle, compared to a placebo condition.

Secondary Objective(s): to assess the acute effects of cannabis on interoception and pain, in females across 3 different phases of the menstrual cycle, compared to a placebo condition.

Tertiary Objective(s): to assess the acute effects of cannabis on metacognition and expression of inflammatory markers in females across 3 different phases of the menstrual cycle, compared to a placebo condition.

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
Double (Participant, Investigator)

盲法说明

Random allocation of participants to the treatment order will be done using Sealed Envelope software, by one experimenter who does not come in direct contact with the participants. The study will be double blind to the subject and the testing experimenter. One experimenter will be respond for preparing the drug treatment. If a subject is withdrawn from the study, the replacement subject will be allocated to the same treatment sequence as the subject they are replacing. Following completion of all data collection the study will be fully unblinded.

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Biological female
  • Used cannabis between 1 time a month and 2 times a week during the previous year
  • Age between 18 and 40 years
  • Free from psychotropic medication
  • Free from hormonal birth control
  • A regular menstrual cycle (last 3 cycles a duration between 21 and 35 days).
  • Good physical health as determined by medical examination and laboratory analysis
  • Absence of any major medical, endocrine and neurological condition as determined by medical examination and laboratory analysis
  • Normal weight, body mass index (weight/height2) between 18 and 28 kg/m2
  • Written Informed Consent
  • Good knowledge and understanding of the English language
  • Participants must be willing to refrain from taking illicit psychoactive substances during the study.
  • Participants must be willing to drink only alcohol-free liquids and no coffee, black or green tea, or energy drinks after midnight of the evening before the study session, as well as during the study day.
  • Participants must be willing not to drive a traffic vehicle or to operate machines within 24 h after substance administration.

排除标准

  • History of drug addiction (determined by the medical questionnaire, drug questionnaire and medical examination)
  • Pregnancy or lactation or pregnancy planned during study participation
  • Hypertension (diastolic > 90 mmHg; systolic > 140 mmHg)
  • Current or history of psychiatric disorder (determined by the medical questionnaire and medical examination)
  • Current presence or history of psychosis in first-degree relatives
  • Any chronic or acute medical condition
  • History of cardiac dysfunctions (arrhythmia, ischemic heart disease,…)
  • Tobacco smoking (>20 per day)
  • Excessive drinking (>20 alcoholic consumptions per week)

研究组 & 干预措施

Cannabis

Experimental

All participants will receive cannabis on 3 separate occasions during different phases of the menstrual cycle.

干预措施: Cannabis (Drug)

Knaster hemp

Placebo Comparator

All participants will receive knaster hemp on 3 separate occasions during different phases of the menstrual cycle.

干预措施: Knaster Hemp (Drug)

结局指标

主要结局

Subjective drug effects

时间窗: Immediately upon inhalation, up to 3.5 hours post administration

Subjective drug effects will be measured via the drug effect questionnaire

THC concentration in blood

时间窗: Baseline (-0.5 hour) and at set time periods up to 3.5 hours post administration

Blood sample will be taken to assess THC concentration in blood.

Retrospective rating of drug effects

时间窗: Immediately upon inhalation, up to 3.5 hours post administration

Retrospective rating of drug effects will be measured via subjective reports on the 5-dimensional altered states of consciousness rating scale

Sensitivity to cannabis reinforcement

时间窗: Immediately upon inhalation, up to 3.5 hours post administration

Measured via the sensitivity to cannabis reinforcement questionnaire,

Marijuana Craving

时间窗: Immediately upon inhalation, up to 3.5 hours post administration

Measured via the marijuana craving questionnaire

Anxiety

时间窗: Immediately upon inhalation, up to 3.5 hours post administration

Measured via the State-Trait anxiety inventory

次要结局

  • Attention(Immediately upon inhalation, up to 3.5 hours post administration)
  • Information processing speed(Immediately upon inhalation, up to 3.5 hours post administration)
  • Verbal Memory(Immediately upon inhalation, up to 3.5 hours post administration)
  • Verbal fluency(Immediately upon inhalation, up to 3.5 hours post administration)
  • Motor Inhibition(Immediately upon inhalation, up to 3.5 hours post administration)
  • Pain threshold(+2.5 hours post administration)
  • Interoception(+1 hr 15 minutes after administration)
  • Subjective experience of pain(+2.5 hours after administration)

研究者

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

Natasha Mason

Assistant Professor

Maastricht University

研究点 (1)

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