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LSD Treatment for Persons With Alcohol Use Disorder (LYSTA)

F

Felix Mueller

Status and phase

Not yet enrolling
Phase 2

Conditions

Alcohol Use Disorder (AUD)

Treatments

Drug: LSD
Drug: Active placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT05474989
2022-00121

Details and patient eligibility

About

Alcohol use causes more overall harm than any other drug and is the seventh leading risk factor for both deaths and disability-adjusted life years. Alcohol use disorders (AUD) are among the most common and undertreated mental disorders in developed countries. Pharmacological and psychotherapeutic treatments only show limited efficacy and around 60% of the patients relapse in the short-term after withdrawal.

Lysergic acid diethylamide (LSD) was investigated in numerous clinical trials during the 1950s and 1960s. Specifically, the use of LSD in the treatment of AUD was investigated extensively. A pooled analysis of six historical clinical trials demonstrated, that a single dose of LSD significantly reduced alcohol use at three and six months after LSD administration. However, these trials are limited by several factors, including the use of diagnostic standards that are no longer not up to date, single, high-dose treatment regimes, missing biological assessment for alcohol use, and no consequent assessment of blinding.

Therefore, the present study aims to evaluate the safety and efficacy of LSD for the treatment of AUD and addresses the shortcomings of previous studies. The trial has a double-blind, active placebo-controlled, randomized, parallel design and will be conducted in specialized treatment centers for addictive disorders in Switzerland. The study will include 126 patients after withdrawal treatment and will primarily assess the efficacy of LSD for the treatment of AUD. Patients will be treated using a 1:1 allocation. Each arm will last 20 weeks and will comprise nine study visits without drug administration and two study days involving LSD or active placebo administration. In the first session, patients in the treatment group will receive a dose of 150 µg LSD, followed by another 150 µg or 250 µg LSD in the second session, which will take place approximately 4 weeks after the first session.

The primary outcome is the mean of percent heavy drinking days after administration of two doses of LSD at 3 months follow-up. Additionally, the study will assess neurobiological mechanisms of action and several other measures.

Enrollment

126 estimated patients

Sex

All

Ages

25+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key inclusion criteria:

  • age ≥ 25 years
  • moderate to severe AUD
  • completion of a qualified detoxification for AUD within 30 days prior to screening
  • a minimum of 4 heavy drinking days within the last 30 days before detoxification
  • intention to stop or decrease drinking

Key exclusion criteria:

  • significant alcohol withdrawal symptoms at screening
  • participating or starting in any formal treatment for AUD until completion of visit 9
  • cognitive impairment
  • borderline personality disorder
  • current post-traumatic stress disorder
  • current suicidality or history of a serious suicide attempt
  • significant prodromal symptoms
  • history of a diagnosis of a psychotic or bipolar disorder in subjects or first-degree relatives
  • pregnancy or breast-feeding
  • lack of safe contraception are exclusion criterion for women only

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

126 participants in 2 patient groups

Verum
Experimental group
Description:
Subjects in the treatment arm will receive 150 μg LSD (first session) and 150 or 250 μg LSD (second session).
Treatment:
Drug: LSD
Active placebo
Active Comparator group
Description:
Subjects in the control arm will receive 10 µg LSD at the first session and 10 µg LSD at the second session.
Treatment:
Drug: Active placebo

Trial contacts and locations

2

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Central trial contact

Felix Müller, PD Dr. med.

Data sourced from clinicaltrials.gov

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