The Effects of Cannabigerol on Attention-Deficit/Hyperactivity Disorder
Recruiting now · Phase 2 · Has a placebo group
Conditions studied: Attention-Deficit/Hyperactivity Disorder
In brief
The goal of this clinical trial is to evaluate the effects of Cannabigerol (CBG) on indicators of Attention-Deficit/Hyperactivity Disorder (ADHD) in a sample of participants indicating/reporting symptoms associated with ADHD. The main question it aims to answer is: Does CBG reduce ADHD-related indicators relative to placebo? Participants will administer an acute dose of placebo or 80mg CBG and complete outcome measures at 45 minutes and 75 minutes. Daily surveys to monitor safety will be administered for one week following administration.
Key facts
- Study ID
- NCT06115603
- Run by
- University of Arkansas, Fayetteville
- People needed
- 76
- Starts
- 2024-12-14
- Expected to finish
- 2026-07-01
- Last updated by the study team
- 2026-05-27
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
Where it is running
- University of Arkansas — Fayetteville, Arkansas, United States (enrolling)
Full record on ClinicalTrials.gov
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