RecruitingPhase 2NCT07210112

Efficacy of Psilocybin and Trazodone Combination in Treatment-resistant Depression: a Randomized Controlled Proof-of-concept Study (PSILOTRAZ)


Sponsor

Centre Hospitalier St Anne

Enrollment

112 participants

Start Date

Jun 30, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Psilocybin, a serotonin receptor agonist in the brain, significantly and quickly improves depressive symptoms while inducing profound acute subjective effects. The benefit-risk ratio of psilocybin in treatment-resistant depression seems favorable, but needs to be confirmed. Moreover, the role of 5-HT2A receptors, involved in the psychedelic experience, on the therapeutic efficacy of psilocybin is still poorly understood. For example, pre-administration of trazodone, a 5-HT2A antagonist antidepressant, could annihilate the acute subjective effects of psilocybin without altering its beneficial effects (Rosenblat et al., 2023). We intend to test this hypothesis by comparing, in a randomized, double-blind, placebo-controlled study, the effect of two possible doses of trazodone (total or partial occupancy of 5-HT2A receptors) on the benefit/risk ratio of psilocybin. We hypothesize that the therapeutic effects of psilocybin are partially independent of 5-HT2A receptor activation and thus persist even after total or partial neutralization of its acute subjective effects.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Placebo of psilocybin, a drug called Placebo of trazodone, and others for people with depression - major depressive disorder and treatment resistant depression (trd). The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPsilocybin 25 mg per os

Caps of psilocybin administered orally once (V3) under medical and psychologist supervision in group 1, 2, and 3 and in an open-label setting for group 4

DRUGTrazodone 5mg

Oral preparation of trazodone administered orally once (V3) with psilocybin in Group 2

DRUGTrazodone 30 mg

Oral preparation of trazodone administered orally once (V3) with psilocybin in Groups 3 \& 4

DRUGPlacebo of psilocybin

Caps of psilocybin placebo will be administered at V3 in group 4

DRUGPlacebo of trazodone

A placebo of trazodone will be administered orally at V3 in group 1


Locations(1)

GHU Paris Psychiatrie and Neurosciences

Paris, France

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NCT07210112


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