Recruiting
Phase 2

Psilocybin & Ketamine

Sponsor:

University of Iowa

Code:

NCT06405607

Conditions

Alcohol Use Disorder

Alcohol Dependence

Alcohol Abuse

Eligibility Criteria

Sex: All

Age: 21 - 65

Healthy Volunteers: Not accepted

Interventions

Psilocybin

Ketamine

Study Details

Brief summary:

This study will collect data that measures the effects of a psychedelic intervention on patients struggling with alcohol use disorder (AUD). The study design will be a double blind, randomized, active-comparator trial with two study arms. Subjects randomized to Arm 1 (n=40) will receive individual psychotherapy sessions plus a 30 mg dose of psilocybin. Arm 2 subjects (n=40) will receive individual psychotherapy sessions and a 0.75 mg/kg dose of ketamine.

Conditions

Alcohol Use Disorder

Alcohol Dependence

Alcohol Abuse

Study ID

NCT06405607

Start date

Jun 12, 2025

Status verified date

Nov, 2025

Completion date

Apr, 2028

Anticipated

Primary completion date

Apr, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 21 - 65

Healthy Volunteers: Not accepted

Inclusion criteria:

  • Weight between 50kg and 150kg
  • No known allergies to rescue medication
  • For people capable of becoming pregnant, not pregnant and using contraception
  • Not currently breastfeeding
  • Meets criteria for DSM-V moderate to severe AUD.
  • Have at least 4 heavy drinking days (5 or more standard drinks in a day) in the past 30 days.
  • Not currently participating in formal treatment for AUD.
  • No history of a of cerebrovascular accident, asthma, or significant alcohol withdrawal history
  • No seizure disorder, coronary artery disease, heart failure, uncontrolled hypertension, insulin-dependent diabetes, pancreatitis, liver disease
  • No hallucinogen or ketamine use in past 12 months
  • No self-reported, personal, or familial history of specific psychotic disorders/episodes.
  • No serious traumatic brain injury (TBI) in the past 2 years
  • No substance use disorder other than AUD over the past 12 months
  • If taking a GLP-1 agonist, stable dosage for past 3 months
  • Family member/friend for pick-up, overnight post-drug session monitoring.
  • No MRI contraindications

Exclusion Criteria:

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).

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 disorder including cocaine, psychostimulant, or opioid use disorder within past 12 months 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.

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), or pregnancy.

MRI contraindication (pacemaker, etc.)

Study Design

Enrollment

80 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Psilocybin Group (Arm 1)

receives individual psychotherapy sessions plus a (30 mg) psilocybin session.

active comparator: Ketamine Group (Arm 2)

receives individual psychotherapy sessions plus a (0.75 mg/kg) ketamine session

Interventions

Psilocybin

30 mg single dose

Ketamine

0.75 mg/kg weight-based single dose

Primary outcome measure

  • Timeline Follow-Back for Alcohol to assess change [ Time Frame: Weekly, over the course of 16 weeks ]

Central Contacts and Locations

Central contacts

Locations

University of Iowa Health Care

Recruiting

Iowa City, Iowa, United States, 52240

Contacts

Lindsay E Golden

lindsay-golden@uiowa.edu

More Information

Sponsor

University of Iowa

Last update posted

Nov 28, 2025

Last verified

Nov, 2025

Keywords

  • psychedelic
  • psilocybin
  • ketamine

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-04. This information was provided to ClinicalTrials.gov by University of Iowa on 2025-11-28.