Acceptability & Safety of Two Sequential Doses of Psilocybin in Bipolar Disorder II Depression and Suicidality
NCT06706232 · The University of Texas Health Science Center, Houston
What it is testing
Summary
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
Feasibility as Assessed by Number of Participants who Complete the Trial (Overall Retention)
Measured over from baseline to 3 weeks after first administration session
Feasibility as Assessed by Number of Therapy Sessions Attended
Measured over from baseline to 3 weeks after first administration session
Feasibility as Assessed by Number of Assessments Completed
Measured over from baseline to 3 weeks after first administration session
Acceptability of Two Dosing Sessions as Assessed by Number of Participants who Choose to Participate in a Second Administration Session
Measured over 11 weeks after first administration session
Acceptability as Assessed by Number of Therapy Sessions Attended
Measured over from baseline to 11 weeks after first administration session
Acceptability as Assessed by Number of Assessments Completed
Measured over from baseline to 11 weeks after first administration session
Score on the Thwarted Belongingness (TB) Items of the Interpersonal Needs Questionnaire (INQ-15)
Measured over baseline, 3 weeks after first administration session
Score on the Perceived Burdensomeness (PB) Items of the Interpersonal Needs Questionnaire (INQ-15)
Measured over baseline, 3 weeks after first administration session
Score on the Columbia-Suicide Severity Rating Scale (C-SSRS)
Measured over baseline, 3 weeks after first administration session
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
Where
1 study site
| Facility | City | Region | Country |
|---|---|---|---|
| The University of Texas Health Science Center at Houston | Houston | Texas | United 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.
NCT06706232 on ClinicalTrials.gov →
Last updated in the registry 2026-08-12. Registry records change; this page reflects the data build of 2026-08-25.
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