drugset / Trial / NCT06115603

The Effects of Cannabigerol on Attention-Deficit/Hyperactivity Disorder

NCT06115603

Phase 2 Recruiting 76 enrolled University of Arkansas, Fayetteville
RandomizedParallel-groupTriple-blindTreatment

Summary

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.

Timeline

Start
2024-12-14
Primary completion
2026-07
Completion
2026-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cannabigerol Small molecule 80 mg