Trials / Recruiting
RecruitingNCT06772753
Investigation of Psychedelic Effects in Psychoactive Substances
- Status
- Recruiting
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Johns Hopkins University · Academic / Other
- Sex
- All
- Age
- 25 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
The aim of this double-blind, placebo-controlled, within-subjects study is to determine whether other psychoactive substances can produce experiences akin to those seen with classic psychedelics. Screening involves a medical and psychiatric examination, including blood draw, history and physical, interviews, and questionnaires. Eligible participants will then be asked to complete up to 6 experimental drug administration session during which the participants will potentially receive and report on the subjective effects of 6 different psychoactive substances or inactive placebo. Drug assignment for some sessions will be randomized (like flipping a count or rolling a pair of dice), and both participants and study staff will be blind to the drug condition on any given day. Participants will also complete 2 preparation sessions (4 hours total) before the first experimental session, and follow-up visits after each session to discuss and debrief on the participants subjective experience.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Placebo | inactive substance |
| DRUG | Psilocybin | active comparator for psychedelic effects |
| DRUG | Ketamine | psychoactive substance |
| DRUG | Dextromethorphan (DXM) | psychoactive substance |
| DRUG | Dimethyltryptamine (DMT) | psychoactive substance |
| DRUG | Methylenedioxymethamphetamine (MDMA) | psychoactive substance |
| DRUG | Tetrahydrocannabinol (THC) | psychoactive substance |
Timeline
- Start date
- 2025-02-05
- Primary completion
- 2027-06-01
- Completion
- 2027-12-01
- First posted
- 2025-01-14
- Last updated
- 2026-02-23
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06772753. Inclusion in this directory is not an endorsement.