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NCT Number: NCT07417059

Sex Hormones Impact on Cannabis Response

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.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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)

Treatment and study plan

Cannabis

Drug

Bedrobinol (13.5% THC) resulting in 300 μg/kg bodyweight THC, administered via a Storz and Bickel Mighty Medic vaporiser.

Other names: Tetrahydrocannabinol

Knaster Hemp

Drug

Placebo will consist of knaster hemp, a freely sold aromatic herbal mixture for smoking. Participants will receive a dose of 50 mg of knaster hemp, administered via a Storz and Bickel Mighty Medic vaporiser.

Primary outcomes

  1. Subjective drug effects

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Subjective drug effects will be measured via the drug effect questionnaire

  2. THC concentration in blood

    Time frame: 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.

  3. Retrospective rating of drug effects

    Time frame: 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

  4. Sensitivity to cannabis reinforcement

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Measured via the sensitivity to cannabis reinforcement questionnaire,

  5. Marijuana Craving

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Measured via the marijuana craving questionnaire

  6. Anxiety

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Measured via the State-Trait anxiety inventory

Secondary outcomes

  1. Interoception

    Time frame: +1 hr 15 minutes after administration

    The Heart rate discrimination task will be used to assess interoception.

  2. Subjective experience of pain

    Time frame: +2.5 hours after administration

    The cold pressor task will be used. Pain is assessed via how many seconds participants can keep their hand in the water.

  3. Attention

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    attention will be assessed via the psychomotor vigilance test

  4. Information processing speed

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Will be assessed via the digit symbol substitution test

  5. Verbal Memory

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Will be assessed via the Immediate and Delayed Verbal Memory Test

  6. Verbal fluency

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Will be assessed via the animal fluency test

  7. Motor Inhibition

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Assessed via the stop signal task

  8. Pain threshold

    Time frame: +2.5 hours post administration

    To assess changes in pain threshold, the pressure pain threshold task will be used.

Other outcomes

  1. Metacognition

    Time frame: Immediately upon inhalation, up to 3.5 hours post administration

    Before and after each task, participants will be shown full text prompts explaining the task, and asking them how well they believe they will do on the task, and upon completion, how well they think they performed.

  2. Inflammatory cytokines

    Time frame: At baseline (-0.5) and 3.5 hours after treatment administration

    Blood samples will be collected to measure inflammatory cytokine levels

Sponsors and collaborators

Lead sponsor

Maastricht University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 18, 2026
Registry last updated
Feb 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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