Phase 2 ADHD Trial, Recruiting NCT06115603 Sponsor: University of Arkansas, Fayetteville Condition: ADHD
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Phase 2 ADHD Trial, Recruiting

NCT06115603
Recruiting Phase 2

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:

  • You are between 18 and 55 years old
  • Your body mass index (BMI) is between 18 and 35 (a measure of body weight relative to height)
  • You scored 4 or above on a standard ADHD self-report questionnaire called the ASRS-v1.1 Part A
  • You have been assessed and meet the recognised criteria for ADHD, with at least mild symptoms, based on a specific diagnostic interview (confirm with trial site)
  • You are not pregnant and are not currently breastfeeding
  • You are willing to use effective contraception (such as the pill, double barrier method, or an IUD) for 30 days before and 30 days after the study
  • You are willing to stop using cannabis or any product containing THC for the entire duration of the study
  • You are willing to keep your current medications the same throughout the study — no starting or stopping treatments
  • You have access to transportation to the University of Arkansas campus for study appointments
  • You are willing to follow any COVID-19 safety guidelines in place at the university (such as wearing a mask)

Who may not be able to join:

  • You are currently pregnant or breastfeeding
  • You have a history of significant allergic reactions to cannabis, cannabinoid medicines, hemp products, medium chain triglyceride oil, or peppermint
  • You have used CBG or any other cannabinoid product in the past 30 days
  • You have ever used a synthetic cannabinoid product, such as dronabinol, nabilone, spice, or K2
  • You have taken part in another clinical trial or used an experimental drug or device in the past 30 days, or plan to do so during this study
  • You are currently taking or have been prescribed ADHD medication in the past six months
  • You are currently having thoughts of suicide
  • You currently have severe major depression or a substance use disorder
  • You have been diagnosed with bipolar disorder or psychosis
  • You currently have an acute illness (such as a respiratory infection) or are taking medication for one (such as antibiotics)
  • You have a history of liver problems or significantly reduced liver function (such as cirrhosis or hepatitis)
  • You have any serious or unstable physical health conditions, including neurological or kidney illness
  • You have any current or past heart or cardiovascular conditions, including low blood pressure, a slow heart rate, or heart block
  • An ECG (heart trace) taken during your visit shows irregular heart rhythms such as atrial fibrillation, slow heart rate, or fast heart rate
  • You have used recreational drugs (other than cannabis) or alcohol in the 12 hours before your in-person study visit
  • You are currently taking any of the following medications: Warfarin, Clobazam, Valproic acid, Phenobarbital, mTOR inhibitors, oral Tacrolimus, St. John's Wort, Epidiolex, Escitalopram, heart or cardiovascular medications, or strong CYP3A4 inhibitors such as Ketoconazole (confirm with trial site if unsure about your medications)

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Ellen W Leen-Feldner, PhD, University of Arkansas

Phone: 4795754256

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

Status
Recruiting
Phase
Phase 2
Sponsor
University of Arkansas, Fayetteville
Registry
ClinicalTrials.gov
Start date
14 December 2024
Est. completion
1 July 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Sustained Attention to Response Task; Trail Making Test-Parts A and B (TMT-A&B); Digit Symbol Substitution Test (DSST); Rey Auditory Verbal Learning Test (AVLT); Iowa Gambling Task (IGT)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov