ACTIVE_NOT_RECRUITING

Psilocybin-Assisted vs Ketamine-Assisted Psychotherapy for Alcohol Use Disorder

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This pilot study will collect preliminary data that measures the effects of psilocybin-assisted psychotherapy vs ketamine-assisted psychotherapy on patients struggling with alcohol use.

Official Title

Psilocybin-Assisted vs Ketamine-Assisted Psychotherapy for Alcohol Use Disorder

Quick Facts

Study Start:2024-02-02
Study Completion:2025-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05421065

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:25 Years to 65 Years
Sexes Eligible for Study:MALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 25-65 years old
  2. * Male
  3. * English fluency
  4. * Meets criteria for DSM-V moderate or severe AUD.
  5. * Have at least 4 heavy drinking days (5 or more standard drinks in a day) in the past 30 days.
  6. * No history of a of cerebrovascular accident, asthma, or significant alcohol withdrawal history
  7. * No seizure disorder, coronary artery disease, heart failure, uncontrolled hypertension, insulin-dependent diabetes
  8. * No current substance use disorder other than AUD
  9. * Negative drug screen (other than THC) on drug administration day
  10. * No prescription medications classified as UGT1A9 inhibitors, UGT1A10 inhibitors, aldehyde or alcohol dehydrogenase inhibitors.
  11. * At least a high-school level of education or equivalent (e.g. GED).
  12. * Lived at current residence for at least 3 months.
  13. * Family member/friend for pick-up, overnight post-drug session monitoring.
  14. * No hallucinogen or ketamine use in past 1 year
  15. * No self-reported, personal, or familial history of specific psychotic disorders/episodes as subjects who take psilocybin may experience a worsening and/or persistent psychotic state. Therefore, these subjects are excluded due to an abundance of caution since even a family history may create a vulnerability to psychosis.
  16. * No serious traumatic brain injury (TBI) in the past 2 years.
  17. * No known allergies to rescue medication (diazepam)
  18. * Weight between 110 and 330 lbs
  1. * Drug/medication assessment that yields: nonprescription medication use, nutritional supplement, or herbal supplement (except when approved by the study investigators), medically unstable, current medication use that has significant potential to interact with study drug (e.g., antidepressants, antipsychotics, psychostimulants, treatments for addictions, other dopaminergic or serotonergic agents, lithium, anticonvulsants, or benzodiazepines).
  2. * Psychiatric assessment that yields:1) history of severe suicide attempt, 2) current suicidality 3) first degree relative with schizophrenia or schizoaffective disorder, 4) comorbid substance use including cocaine, psychostimulant, or opioid use disorder within past 12 months and/or any use within past 30 days, 5) history of co-occurring psychotic episode/diagnosis including schizophrenia, schizoaffective disorder, schizophreniform, substance-induced psychosis, delusional disorder, or psychosis not otherwise specified, 6) high risk of adverse emotional or behavioral reaction based on the medical monitor's clinical evaluation that may also yield evidence of serious current stressors, a lack of meaningful social support, antisocial behavior, and/or serious personality disorders amongst other conditions.
  3. * Medical assessment that yields: serious ECG abnormalities (evidence of ischemia, myocardial infarction, QTc prolongation \[QTc \> .045\]), serious abnormalities of complete blood count or chemistries, medical conditions that would preclude safe participation (significantly impaired liver function).
  4. * MRI contraindication (pacemaker, etc.)

Contacts and Locations

Principal Investigator

Peggy C Nopoulos, MD
PRINCIPAL_INVESTIGATOR
University of Iowa

Study Locations (Sites)

University of Iowa
Iowa CIty, Iowa, 52242
United States

Collaborators and Investigators

Sponsor: Peggy C Nopoulos

  • Peggy C Nopoulos, MD, PRINCIPAL_INVESTIGATOR, University of Iowa

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-02
Study Completion Date2025-09

Study Record Updates

Study Start Date2024-02-02
Study Completion Date2025-09

Terms related to this study

Keywords Provided by Researchers

  • psilocybin
  • ketamine

Additional Relevant MeSH Terms

  • Alcohol Use Disorder