Efficacy in Relapse Prevention: Psilocybin in Alcohol Use Disorder With Depressive Symptoms

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de Nīmes

About this trial

Up to 40% of individuals with alcohol use disorder (AUD) experience depression, which increases the risk of early relapse. Depression can cause relapse to occur 3 times faster in individuals with AUD who experience depressive symptoms at discharge. No treatments have been approved for individuals with both AUD and depression. Psilocybin, a psychedelic, shows promising results in treating both depression and addiction. It may be particularly effective for preventing relapse in people with AUD who also have depressive symptoms after detoxification, offering quicker action than traditional antidepressants.

The Psilocybin Alcohol Depression (PAD) pilot study, launched in February 2024, has provided critical insights for avoiding methodological flaws and demonstrated that psilocybin-assisted psychotherapy (PAP) is both feasible and acceptable. Preliminary efficacy analyses were conducted: at 12 weeks, the 25 mg group showed significantly greater reductions in drinking days (p = 0.038) and craving frequency (p = 0.045). Relapse rates were 35% in the 25 mg group and 50% in the control group (HR = 0.52 \[0.16-1.65\]). In the ERPPAD trial, the study authors will compare high-dose PAP with low-dose PAP in preventing relapse in individuals with AUD and depressive symptoms. The hypothesis is that high-dose PAP will be more effective than low-dose in preventing relapse over 6 months.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Confirmed DSM-5 diagnosis of severe AUD.

Scale BDI-II ((Beck Depression Inventory) ≥14

The last drink must have been consumed between day(D) -60 and D -10 at the inclusion visit. The patient must have had at least 1 HDD during the last drinking period NB: The last drinking period before inclusion is defined by the last 4 weeks counted from the last drink.

The patient must have given their free and informed consent and signed the consent form

Disqualifiers

The subject is participating in an interventional study, a clinical trial, or a clinical investigation or is in a period of exclusion determined by a previous study

The subject refuses to sign the consent

It is impossible to give the subject informed information

The patient is under safeguard of justice or state guardianship

Trial design

Design model

Parallel

Treatments tested in this trial

  • Psilocybin (high dose)

    Drug

    2 administrations of high-dose psilocybin (25 mg) 3 weeks apart

  • Psilocybin (low dose)

    Drug

    2 administrations of low-dose psilocybin (3 mg) 3 weeks apart

Treatment groups

172 Participants
are divided into 2 treatment groups
Group A: High dose psilocybinExperimental treatment 1 intervention
Group B: Low-dose psilocybinPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Incidence of relapse between groups

Relapse Yes/no, where relapse is defined as the 1st heavy drinking day, assessed using the Timeline Follow-Back (TLFB) method

Time frame
Month 6
2

Time to relapse between groups

Days until relapse, where relapse is defined as the 1st heavy drinking day, assessed using the Timeline Follow-Back (TLFB) method

Time frame
Month 6

Secondary outcomes

1

Change in relapse rate between groups

Assessed using the Timeline Follow-Back (TLFB) method

Time frame
At weeks 3, 9, 15, 21, 27 compared to baseline
2

Change in rate of heavy drinking days between groups

Percent; Assessed using the Timeline Follow-Back (TLFB) method

Time frame
At weeks 3, 9, 15, 21, 27 compared to baseline
3

Change in total alcohol consumption between groups

Grams, assessed using the Timeline Follow-Back (TLFB) method

Time frame
At weeks 3, 9, 15, 21, 27 compared to baseline
4

Change in number of drinking days between groups

Days, assessed using the Timeline Follow-Back (TLFB) method

Time frame
At weeks 3, 9, 15, 21, 27 compared to baseline

Other outcomes

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