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Cannabis oil study probes Brain's stress response

NCT ID NCT05261321

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at how different types of cannabis oil (high or low CBD-to-THC ratio) affect stress and self-control in healthy adults aged 19-35 who use cannabis occasionally. Participants will undergo brain scans and stress tests to measure changes in brain activity, stress hormones, and impulse control. The goal is to understand the neurological effects of cannabis, not to treat any disease.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

About 20 people

The number the study aims to enrol. It can still change while the study runs.

Started

Oct 2022

Expected to finish

Mar 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

19 to 35 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion criteria: 1. Are 19-35 years old at the start of the study 2. Have used oral cannabis, including at least 5mg of THC, at least once in their life 3. Have used cannabis at least once in the past year 4. Used cannabis less than 3 times per week on average, in the past 3 months 5. Are using an effective and/or highly effective method of contraception and will continue to do so for the duration of participation in the study. Health Canada's definition of effective methods of contraception include barrier methods of contraception (e.g. male condom, female condom, cervical cap, diaphragm, contraceptive sponge). Health Canada's definition of highly effective methods of contraception includes hormonal contraceptives (e.g. combined oral contraceptives, patch, vaginal ring, injectables, and implants); intrauterine device (IUD) or intrauterine system (IUS); vasectomy and tubal ligation. 6. Females: are not undergoing alternative fertility methods, such as IVF, or otherwise trying to start a family for the duration of participation 7. Males: will not be donating sperm at some point during the duration of participation 8. Are able to provide informed consent 9. Are able to complete assessments in English 10. Are able to attend sessions according to the study schedule 11. Will provide proof of 2 doses of an approved COVID-19 vaccination Exclusion criteria: 1. Are left-handed or ambidextrous 2. Females: are pregnant, nursing, or not on safe pregnancy protection 3. Are trying to conceive 4. Have a known or suspected allergy to cannabinoids and/or palm/coconut oil 5. Are hypersensitive to CBD and/or THC and/or have ever had an adverse reaction (an unwanted and unexpected reaction), to less than 40mg of CBD and/or 10mg THC 6. Have had an adverse reaction (unwanted, unexpected reaction or symptoms) to cannabis within last 6 months 7. Have a major physical problem/health concern, including: 1. Liver-cirrhosis or other liver disease 2. Diabetes 3. Chronic illness that may increase risk for adverse reactions to cannabis 4. Chronic pain 5. Genetic glucuronidation disorders (e.g., Gilbert's disease) 6. Cardiovascular disease, including ischemic heart disease with unstable angina or recent acute coronary syndrome in the last 3 months, uncontrolled arrhythmias, poorly controlled hypertension or high blood pressure (e.g., 130/80), or severe heart failure 7. Delirium: active delirium or recent delirium \< 7 days, or at significant risk of delirium due to multiple comorbidities (e.g., very elderly, cognitive impairment, cerebrovascular disease) and contributing drugs (e.g., alcohol, stimulants, high doses of benzodiazepines, opioid, sedatives, psychoactive medications) 8. Are taking any of the following medications: 1. Any medication that impacts the central nervous system, brain, and/or metabolic system 2. Psychotropic medications, sedatives, and central nervous system depressants, including sleeping pills, tranquilizers, some pain medications, some allergy and cold medications, and anti-seizure medications 3. Medications otherwise affecting the central nervous system, including amphetamines and other sympathomimetics 4. Allergy medications (antihistamines; within 24 hours) 5. Heart medications 6. Blood pressure medication 7. Steroid medications 8. Opioids or other pain medications 9. Anticholinergics: drugs that block acetylcholine, a chemical signal that plays a role in memory and learning. 10. Drugs metabolized by cytochrome P450 enzymes, including amitriptyline, fentanyl, sufentanil, and alfentanil 11. Highly protein-bound drugs, including warfarin, cyclosporine, and amphtericin 12. Drugs metabolized by UGT enzymes, including propofol, antivirals 13. Antiretroviral drugs 14. Stomach acid inhibitors 15. Antibiotics and antifungal medications 16. Heart medications 17. Other medications/substances interfering with CYP2C19 receptors i. Inhibitors: Fluvoxamine, isoniazid (INH), ritonavir ii. Inducers: Carbamazepine, phenytoin, rifampin iii. Substrates: Omeprazole (Prilosec), phenobarbital, phenytoin r. Other medications/substances interfering with CYP3A4 receptors: i. Inhibitors: Clarithromycin (Biaxin), diltiazem (Cardizem), erythromycin, grapefruit juice, itraconazole (Sporanox), ketoconazole (Nizoral), nefazodone (Serzone), ritonavir, telithromycin (Ketek), verapamil (Calan) ii. Inducers: Carbamazepine, Hypericum perforatum (St. John's wort), phenobarbital, phenytoin, rifampin iii. Substrates: Alprazolam (Xanax), amlodipine (Norvasc), atorvastatin (Lipitor), cyclosporine (Sandimmune), diazepam (Valium), estradiol (Estrace), simvastatin (Zocor), sildenafil (Viagra), verapamil, zolpidem (Ambien) 9. Other MRI contraindications (conditions that make MRI procedure inadvisable): a. Have implanted metal clips or wires, including: i. Implanted electronic device (e.g., pacemaker, defibrillator implanted medication infusion pump, electrical stimulator, and/or ear or eye implant) including retained wires that has been removed (e.g., pacemaker wires not attached to a pacemaker) ii. Stainless steel intrauterine device (IUD) iii. Metal in eye or orbit, or metal slivers iv. Ferromagnetic aneurysm clip v. Coil, catheter, or filter in any blood vessel vi. Orthopedic hardware (artificial joint, plate, screw, rod) vii. Shrapnel, bullets, or other metal fragments (i.e., metal in eye or orbit) viii. Artificial heart valve ix. Ear or eye implant x. Brain aneurysm clip xi. Implanted electronic device (i.e., drug infusion pump, electrical stimulator) xii. Coil, catheter, or filter in any blood vessel xiii. Surgery, medical procedure or tattoos (including tattooed eyeliner) in the last six weeks xiv. Other metallic prostheses b. Have a personal or family history of seizures c. Have any significant neurological disorder including, but not limited to: i. Any condition likely to be associated with increased intracranial pressure ii. Space-occupying brain lesion iii. Seizure iv. Cerebral aneurysm v. Parkinson's disease vi. Huntington's chorea vii. Multiple sclerosis viii. Significant head trauma with loss of consciousness for greater than or equal to 5 minutes d. Claustrophobia (i.e., feel uncomfortable in small spaces) or fear of loud, repetitive sounds, or inability to lay still. Participants will have to lie still in the confined space of the MRI scanner. 10. Work nightshifts 11. Have any diagnosed sleep disorders 12. Have dyscalculia 13. Have a neurodevelopmental disorder or cognitive impairments, including: 1. Autism Spectrum Disorder 2. Attention Deficit/Hyperactivity Disorder (ADHD) 14. Have schizophrenia spectrum disorder and/or history of psychosis 15. Meet criteria for potential mental health disorder in the Mini International Neuropsychiatric Interview (M.I.N.I.) Screen Version 7.0.2, except for alcohol and cannabis use disorders 16. Any diagnosed current mental health disorder and/or diagnosis of a mental health disorder within the past year 17. Have a non-correctable clinically significant sensory impairment (e.g., cannot hear well enough to cooperate with interview) 19\) Are unable to attend sessions according to the study schedule 20) Have used opiates more than twice in the past 30 days

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • B.R.A.I.N. Lab, Institute of Mental Health, Faculty of Medicine, University of British Columbia

    Vancouver, British Columbia, V6T 1Z3, Canada

More trials for these conditions

Other studies related to the condition(s) this trial covers.