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WithdrawnPhase 2

PET Synaptogenesis After Psilocybin In DEpression Recovery

NCT05601648 · PET-SPIDER · Washington University School of Medicine

Closed to entry
Status
Not accepting participants
Phase 2
Phase
Target enrolment
1
Study sites
1 US states

What it is testing

Summary

Participants with depression will be given a single dose of psilocybin and supportive psychotherapy before, during, and after drug administration. Participants will undergo positron emission tomography (PET) imaging before and one week after psilocybin using a marker of synaptic density. This design allows us to assess the relationship between neurotrophic, and antidepressant effects produced by psilocybin.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Synaptogenesis in hippocampus

    Measured over 7 days after psilocybin

  • Synaptogenesis in medial prefrontal cortex

    Measured over 7 days after psilocybin

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years to 65 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: 1. Men and women between 18 and 65 years of age; 2. Able to provide informed consent 3. Women of childbearing age must agree to be on two forms of contraception and men are required to utilize at least one form of contraception 4. Willingness to comply and be available for all study requirements, including psychological, cognitive, and imaging for the duration of the study 5. Meeting DSM-5 criteria for major depressive disorder and current depressive episode 6. Snaith-Hamilton Anhedonia Pleasure Scale (SHAPS) ≥ 6 points 7. Willing and able to taper and/or discontinue current psychotropic medications Exclusion Criteria: 1. Women who are pregnant or who intend to become pregnant or nurse during the study duration. 2. Presence of psychiatric conditions that are contraindications to psilocybin exposure (e.g., personal or first degree relative with history of schizophrenia spectrum or bipolar disorder); 3. Use of psychotropic medication that may interact with psilocybin (TCA, MAOi, antipsychotic/neuroleptics, anti-epileptic/mood stabilizer, lithium, SSRI, SNRI, Mirtazapine, Buproprion, Vortioxetine). 4. Recent use of psychedelics (psilocybin, LSD, ayahuasca, mescaline; past 5 years); or prior severe adverse reactions to psychedelics 5. Active suicidal ideation or history of a suicide attempt. 6. Presence of medical conditions that are contraindications to psilocybin exposure (e.g., neurological conditions or severe hypertension, severe and/or unstable metabolic or cardiovascular conditions); 7. Current medical conditions that are known to increase risk of severe coronavirus infection or deemed by a study physician to put an individual at high risk (i.e., cancer, COPD, obesity, immunosuppression, type 2 diabetes, serious heart conditions, sickle cell disease, asthma); 8. Presence of contraindications to PET or MRI scanning (renal disease, implantable devices, bone hardware, some IUDs); 9. Body mass index \>30 (due to MRI confounds).

Where

1 study site

FacilityCityRegionCountry
Washington University School of MedicineSt LouisMissouriUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT05601648 on ClinicalTrials.gov →

Last updated in the registry 2023-01-30. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits