Phase 2 Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are at least 60 years old
- People who are able to give informed consent (formally agree to take part in the study)
- People who have tried a cannabis product at least once in the past with no negative effects
- People who have not been using cannabis products regularly (fewer than 3 times per month) in the last 6 months
- Female participants must be postmenopausal (have gone through menopause)
- People whose liver function test results (specific markers called ALT and AST) are within an acceptable range for their age
- People who are currently taking medication for pain, sleep, and/or mood
Who may not be able to join:
- People who have any alcohol in their system at the screening appointment (the initial visit to sign consent forms)
- People who have used cocaine, opiates, or methamphetamine in the past 90 days, or whose urine test shows signs of these substances
- People who have a personal or family history of psychosis (a condition involving a loss of contact with reality), whether past or current
- People who are currently taking anti-epileptic medications (such as clobazam or sodium valproate)
- People who are currently taking certain medications known to interact with the study drug Epidiolex, including buprenorphine, leflunomide, levomethadyl acetate, lomitapide, mipomersen, pexidartinib, propoxyphene, sodium oxybate, and/or teriflunomide (confirm with trial site if unsure about a specific medication)
- People who are currently taking antipsychotic medications
- People who are currently undergoing chemotherapy
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 6037697718
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Subjective Motor Function; Balance; Anxiety; Depression; Blood Cytokine Levels; Depression/Anxiety; Drug Effects; Inhibitory Control; Cognitive Function; Pain Intensity and Interference; Cognitive Ability; Pain Intensity; Change in Condition; Sleep Disturbance; Sleep-Related Impairment; Memory
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.