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RECRUITING
NCT06115603
PHASE2

The Effects of Cannabigerol on Attention-Deficit/Hyperactivity Disorder

Sponsor: University of Arkansas, Fayetteville

View on ClinicalTrials.gov

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.

Official title: CBG and Attention: A Double-Blind, Randomized, Placebo-Controlled Trial Examining the Effects of Cannabigerol on Indicators of Attention-Deficit/Hyperactivity Disorder

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

76

Start Date

2024-12-14

Completion Date

2025-12

Last Updated

2025-04-02

Healthy Volunteers

Yes

Interventions

DRUG

Cannabigerol

1 mL of 80mg Cannabigerol once during experimental session

OTHER

Placebo

1 mL of placebo once during experimental session

Locations (1)

University of Arkansas

Fayetteville, Arkansas, United States