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Active (not recruiting) Phase 1/2 NCT04982796

Psilocybin-Enhanced Psychotherapy for Methamphetamine Use Disorder

Phase 1/2 – combined early trial
Conditions: Amphetamine-Related Disorders

Sponsor: Portland VA Research Foundation, Inc

trial.available_in: БГ
Overview
This is a proof-of-concept randomized clinical trial of psilocybin-enhanced psychotherapy versus treatment-as-usual among individuals being treated for methamphetamine use disorder.
Description
The trial will take place with individuals admitted to a residential rehabilitation treatment program. The treatment protocol will consist of 4 preparatory therapy visits, 2 psilocybin sessions (25-30mg), and 8 total integration therapy visits. Primary aims assess acceptability, feasibility, and safety with a primary endpoint at the conclusion of the study intervention. An additional aim assesses preliminary efficacy for methamphetamine use disorder and overall functioning at follow-up assessments 60 and 180 days after discharge from the residential treatment program.
Who can participate
Inclusion Criteria: * United States military Veteran * Moderate to severe methamphetamine use disorder using the DSM-V diagnostic criteria * Desire to cease or reduce methamphetamine use Exclusion Criteria: * Have uncontrolled hypertension or clinically significant cardiovascular disease * History of seizure disorder in adulthood * CNS metastases or symptomatic central nervous system (CNS) infection * Poorly controlled diabetes mellitus * Taking certain medications that may interact with psilocybin * History of any primary persistent psychotic disorder, including schizophrenia, schizoaffective disorder, bipolar disorder with psychosis, major depressive disorder with psychosis, or schizophreniform disorder * History of bipolar I disorder * Current eating disorder with active purging * History of hallucinogen use disorder * Pregnant or breast feeding
Interventions
Psilocybin
DRUG
Treatment-as-usual
BEHAVIORAL
Locations 1
United States (1)
Portland VA Health Care System
Vancouver , Washington
Technical details
Status
Active (not recruiting)
Phase
Phase 1/2
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
25 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
07.07.2022
Completion date
31.12.2026
Registry ID
NCT04982796
Source
clinicaltrials.gov
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