Neural Effects of Intravenous N,N-dimethyltryptamine (DMT)

Part of paid clinical trials in La Jolla, California.

Sponsor
Jon Dean
Study ID
NCT07693257
Phase
PHASE1
Status
Not Yet Recruiting

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Conditions

  • Healthy Participants Study

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Accepted

Interventions

  • N,N-Dimethyltryptamine (15 mg) — DRUG
    Participants will receive one "low" dose (15 mg for 1 min + 1.5 mg/min for 59 min) of synthetic DMT (hemifumarate) via IV injection.
  • N,N-Dimethyltryptamine (17.5 mg) — DRUG
    Participants will receive one "medium" dose (17.5 mg for 1 min + 1.75 mg/min for 59 min) of synthetic DMT (hemifumarate) via IV injection.

Study Details

This study examines how the psychedelic substance DMT affects the human brain when administered by the intravenous (IV) route. DMT is a naturally occurring chemical in the body that is thought to help improve mood when ingested in a continuously monitored medical setting. Previous research has shown that a single IV injection of DMT can be given safely, but its effects, which include changes in perception, emotions, and thinking, usually wear off within 15-20 minutes. To better understand what happens when DMT's effects last longer, researchers have developed a method to give DMT slowly and continuously through an IV, which safely extends its effects for up to an hour or more. In this study, healthy volunteers who have prior experience using DMT will receive low and medium doses of DMT in this extended manner through an IV for 1 hour while undergoing a brain scanning technique known as functional magnetic resonance imaging (fMRI). These scans allow researchers to see changes in brain activity and blood flow in real time. Participants will complete psychological assessments before and after receiving DMT, and additional brain scans without DMT will be used for comparison. The researchers will also use advanced computer techniques to help identify brain patterns linked to the visual experiences people report during DMT. Overall, the goal of the study is to better understand how DMT affects the brain during an extended experience and to learn more about the biological processes behind its psychological effects.

Key Dates

First listed
Jul 9, 2026
Start date
Sep 1, 2026
Status verified
Jul 2026
Primary completion
Sep 1, 2028
Completion
Sep 1, 2029

Study Design

Enrollment
20 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE

Arms

  • Experimental: DMT hemifumarate "low" dose
    Participants will be randomized to receive, in a double-blinded, counter-balanced, and crossover design, two doses of IV DMT during fMRI scanning delivered within two weeks apart under the care of a study physician.
  • Experimental: DMT hemifumarate "medium" dose
    Participants will be randomized to receive, in a double-blinded, counter-balanced, and crossover design, two doses of IV DMT during fMRI scanning delivered within two weeks apart under the care of a study physician.

Primary Outcome Measure

fMRI - Blood Oxygen Level Dependent (BOLD) Signaling [ Time Frame: Up to 3 months: Assessed at baseline fMRI (Visit 2) and dosing fMRI (Visits 6, 8). ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Altman Clinical and Translational Research InstituteLa JollaCalifornia92037
Jon Dean, PhD (PRINCIPAL_INVESTIGATOR)

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