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Recruiting Phase 1 NCT06070649

NCT06070649 The Potential Therapeutic Effects of Psychedelic, N, N-dimethyltryptamine (DMT), on Alcohol Use Disorder (AUD)

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Clinical Trial Summary
NCT ID NCT06070649
Status Recruiting
Phase Phase 1
Sponsor Yale University
Condition Alcohol Use Disorder (AUD)
Study Type INTERVENTIONAL
Enrollment 63 participants
Start Date 2025-08-04
Primary Completion 2027-08-01

Eligibility & Interventions

Sex All sexes
Min Age 21 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
0.3mg/kg/min Dimethyltryptamine + Normal Saline infusion0.2 mg/kg/min + Dimethyltryptamine 0.01mg/kg/min infusion25 mg Diphenhydramine (5 min) + Normal Saline

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 63 participants in total. It began in 2025-08-04 with a primary completion date of 2027-08-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This proposed study is a double-blind, randomized, placebo-controlled, parallel-group, laboratory study to determine the effects of DMT, plus psychotherapy, on Alcohol Use Disorder.

Eligibility Criteria

Inclusion Criteria: * Diagnostic and Statistical Manual of Mental Disorders-5th edition (DSM-5) diagnosis of Alcohol Use Disorder * Medically healthy * Ability to provide consent Exclusion Criteria: * Unstable medical conditions

Contact & Investigator

Central Contact

Angelina Contreras

✉ angelina.contreras@yale.edu

📞 (203) 974-7525

Principal Investigator

Anahita Bassir Nia, MD

PRINCIPAL INVESTIGATOR

Yale University

Frequently Asked Questions

Who can join the NCT06070649 clinical trial?

This trial is open to participants of all sexes, aged 21 Years or older, up to 65 Years, studying Alcohol Use Disorder (AUD). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06070649 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT06070649 currently recruiting?

Yes, NCT06070649 is actively recruiting participants. Contact the research team at angelina.contreras@yale.edu for enrollment information.

Where is the NCT06070649 trial being conducted?

This trial is being conducted at New Haven, United States.

Who is sponsoring the NCT06070649 clinical trial?

NCT06070649 is sponsored by Yale University. The principal investigator is Anahita Bassir Nia, MD at Yale University. The trial plans to enroll 63 participants.

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