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RecruitingNCT06927076

Antidepressant Response of DMT Masked With Propofol

Trial Parameters

ConditionMajor Depressive Disorder
SponsorUniversity Hospital, Basel, Switzerland
Study TypeINTERVENTIONAL
PhaseN/A
Enrollment112
SexALL
Min Age21 Years
Max AgeN/A
Start Date2025-08-05
Completion2029-03
Interventions
N,N-DimethyltryptaminePlaceboPropofol

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Brief Summary

The aim of this study is to elucidate if the anti-depressive effect of N,N-dimethyltryptamine (DMT) is based on a biological mechanisms including neuroplasticity and anti-inflammatory effect or due to the subjective psychedelic experience.

Eligibility Criteria

Inclusion Criteria: 1. Participants must meet DSM-5 criteria for MDD of at least moderate severity (MADRS≥20). 2. Participants either currently do not use antidepressants or are treated with a stable dose for at least 4 weeks prior to randomization. 3. Age ≥ 21 years old. 4. Sufficient understanding of the German language. 5. Able to understand the study procedures and risks and willing to adhere to the protocol and sign the consent form. 6. Willing not to drive or operate heavy machinery on the treatment day. 7. Willing to refrain from more than 7 standard alcoholic drinks a week, more than 10 cigarettes a day, more than 2 cups of coffee a day, and any illicit substances during study participation. 8. Willing to use effective contraceptive measures throughout study participation. Exclusion Criteria: 1. Past or present bipolar or psychotic disorder, including depressive disorder with psychotic features. 2. First-degree relative with a psychotic or bipolar disorder. 3. Significant prodr

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