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Cannabinoid
Inhaled THC for Cannabis Response Differences by Gender (THC-Gender-II Trial)
Phase 1
Recruiting
Research Sponsored by Yale University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and +80 minutes after start of oral dronabinol administration.
Summary
This trial examines how inhaling THC affects women compared to men and explores why these differences might exist.
Who is the study for?
This trial is for healthy men and women who have tried cannabis at least once. It's not suitable for those who've never used cannabis or are currently dealing with major stress.
What is being tested?
The study is looking into how inhaled THC (the active ingredient in cannabis) affects men and women differently by comparing it to a placebo, which has no active ingredients.
What are the potential side effects?
While the side effects aren't listed, typical reactions to THC may include altered senses, mood changes, difficulty with thinking and problem-solving, impaired memory, and occasionally anxiety.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and +80 minutes after start of oral dronabinol administration.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and +80 minutes after start of oral dronabinol administration.
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change from Baseline: Rewarding Effects measured by Visual Analog Scale (VAS)
Change from Baseline: Verbal Learning: Measured by Rey Auditory Verbal Learning Test (RAVLT)
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Delta-9-Tetrahydrocannabinol (THC)Active Control1 Intervention
4 mg vaporized THC will be administered.
Group II: PlaceboPlacebo Group1 Intervention
Inhaled placebo (no active cannabinoids)
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Cannabis treatments primarily interact with the endocannabinoid system, which includes CB1 and CB2 receptors, endogenous cannabinoids, and related enzymes. THC binds to CB1 receptors in the brain, producing psychoactive effects and pain relief, while CBD modulates THC's effects and interacts with other receptors like serotonin and TRPV1.
Understanding these mechanisms is crucial for patients as it affects the therapeutic benefits and side effects of cannabis, impacting its use in managing chronic pain, multiple sclerosis, and cancer-related symptoms.
Cannabinoid pharmacology.Understanding <i>Cannabis sativa</i> L.: Current Status of Propagation, Use, Legalization, and Haploid-Inducer-Mediated Genetic Engineering.
Cannabinoid pharmacology.Understanding <i>Cannabis sativa</i> L.: Current Status of Propagation, Use, Legalization, and Haploid-Inducer-Mediated Genetic Engineering.
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Yale UniversityLead Sponsor
1,920 Previous Clinical Trials
3,040,295 Total Patients Enrolled
14 Trials studying Cannabis
724 Patients Enrolled for Cannabis
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You are experiencing a lot of stress right now or have recently experienced a major life event.I am in good physical and mental health.You have used cannabis at least once in your life.People who have never used cannabis before.
Research Study Groups:
This trial has the following groups:- Group 1: Delta-9-Tetrahydrocannabinol (THC)
- Group 2: Placebo
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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