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Phase 2 Completed N=95 Randomized Quadruple-blind Treatment

A Double-Blind Trial of Psilocybin-Assisted Treatment of Alcohol Dependence

Source: ClinicalTrials.gov NCT02061293 ↗
Enrolled (actual)
95
Serious AEs
2.2%
Results posted
Oct 2022
Primary outcomePrimary: Percent of Heavy Drinking Days — 56.48; 48.57 percentage of days

Summary

Several lines of evidence suggest that classic hallucinogens such as psilocybin can facilitate behavior change in addictions such as alcohol dependence. The proposed investigation is a multi-site, double-blind active-controlled trial (n = 180, 90 per group) contrasting the acute and persisting effects of psilocybin to those of diphenhydramine in the context of outpatient alcoholism treatment.

Outcome Measures

OutcomeResultp-value
PRIMARY
Percent of Heavy Drinking Days
9.71; 23.57
PRIMARY
Percent of Heavy Drinking Days
9.71; 23.57
PRIMARY
Percent of Heavy Drinking Days
9.71; 23.57
PRIMARY
Drinks Per Day
1.17; 2.26
PRIMARY
Drinks Per Day
1.17; 2.26
PRIMARY
Drinks Per Day
1.17; 2.26
PRIMARY
Percent of Drinking Days
29.39; 42.83
PRIMARY
Percent of Drinking Days
29.39; 42.83
PRIMARY
Percent of Drinking Days
29.39; 42.83
SECONDARY
Short Inventory of Problems (SIP-2R) Score
6.59; 13
SECONDARY
Short Inventory of Problems (SIP-2R) Score
6.59; 13
SECONDARY
Percentage of Participants Achieving Abstinence From Drinking
47.9; 24.4
SECONDARY
Percentage of Participants Achieving Abstinence From Drinking
47.9; 24.4
SECONDARY
Percent of Participants Achieving No Heavy Drinking Days
62.5; 40
SECONDARY
Percent of Participants Achieving No Heavy Drinking Days
62.5; 40
SECONDARY
Percent of Participants Achieving WHO Risk Drinking Level Decrease of at Least 1 Level
89.6; 64.4
SECONDARY
Percent of Participants Achieving WHO Risk Drinking Level Decrease of at Least 1 Level
89.6; 64.4
SECONDARY
Percent of Participants Achieving WHO Risk Drinking Level Decrease of at Least 2 Levels
60.4; 40
SECONDARY
Percent of Participants Achieving WHO Risk Drinking Level Decrease of at Least 2 Levels
60.4; 40
SECONDARY
Percent of Participants Achieving WHO Risk Drinking Level Decrease of at Least 3 Levels
37.5; 17.8
SECONDARY
Percent of Participants Achieving WHO Risk Drinking Level Decrease of at Least 3 Levels
37.5; 17.8

Eligibility Criteria

Inclusion Criteria

  • Males and females age 25-65 with SCID (DSM-IV) diagnosis of alcohol dependence who
  • Want to stop or decrease their drinking
  • Are not participating in any formal treatment for alcohol dependence (12-step meetings are not considered treatment)
  • Are able to provide voluntary informed consent
  • Have at least 4 heavy drinking days in the past 30 days
  • If female of childbearing potential, are willing to use approved form of contraception from screening until after the psilocybin administration sessions
  • Have a family member or friend who can pick them up and stay with them overnight after the psilocybin administration sessions
  • Are able to provide adequate locator information.

Exclusion Criteria

  • Medical conditions that would preclude safe participation in the trial (e.g., seizure disorder, significantly impaired liver function, coronary artery disease, heart failure, uncontrolled hypertension (above 165/95 mmHg at screening), history of cerebrovascular accident, asthma, hyperthyroidism, narrow-angle glaucoma, stenosing peptic ulcer, pyloroduodenal obstruction, symptomatic prostatic hypertrophy, or bladder-neck obstruction)
  • Exclusionary psychiatric conditions (schizophrenia, schizoaffective disorder, bipolar disorder, current major depressive episode, current post-traumatic stress disorder, current suicidality or history of medically serious suicide attempt)
  • Cognitive impairment (Folstein Mini Mental State Exam score 25 lifetime uses;
  • Cocaine, psychostimulant, opioid, or cannabis dependence (past 12 months)
  • Current non-medical use of cocaine, psychostimulants, or opioids (past 30 days)
  • Significant alcohol withdrawal (CIWA-Ar score greater than 7. Patients presenting at screening in withdrawal may be referred for detoxification and reassessed within 30 days)
  • Serious ECG abnormalities (e.g., evidence of ischemia, myocardial infarction, QTc prolongation [QTc > .045 for men, QTc > .047 for women])
  • Serious abnormalities of complete blood count or chemistries
  • Active legal problems with the potential to result in incarceration
  • Pregnancy or lactation
  • Need to take medication with significant potential to interact with study medications (e.g., antidepressants, antipsychotics, psychostimulants, treatments for addictions, other dopaminergic or serotonergic agents, lithium, anticonvulsants).
  • Allergy or hypersensitivity to psilocybin or diphenhydramine.
  • High risk of adverse emotional or behavioral reaction based on investigator's clinical evaluation (e.g., evidence of serious personality disorder, antisocial behavior, serious current stressors, lack of meaningful social support).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02061293). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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