Psilocybin for Chronic Pelvic Pain (CPP) in Women: A Pilot Feasibility Study
Sponsor: Oregon Health and Science University • ClinicalTrials.gov ID: NCT06988319
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The primary aim is to determine the feasibility of enrolling and 15 women with chronic pelvic pain (CPP) that have failed one conventional for CPP to obtain preliminary safety data on a single administration of a moderate dose of pharmaceutical grade psilocybin (25 mg) in combination with psychotherapy sessions (two pre-dose preparatory and three post-dose integration sessions).
Interventions
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Psilocybin (Usona Institute)
(Drug)
Single dose of pharmaceutical grade psilocybin (25 mg) combined with psychotherapy sessions
Eligibility criteria
Conditions
Locations
- Oregon Health & Science University — Portland, Oregon, United States
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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