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First study of safety and tolerability of 3,4-methylenedioxymethamphetamine-assisted psychotherapy in patients with alcohol use disorder.
2021
|
open-label proof-of-concept study |
14 |
↑Supports
|
MDMA-assisted psychotherapy (two 187.5 mg sessions) was well tolerated with no unexpected adverse events, psychosocial functioning improved, and average alcohol consumption fell from 130.6 to 18.7 units per week nine months after detox, described by the authors as preliminary. |
|
First study of safety and tolerability of 3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy in patients with alcohol use disorder: preliminary data on the first four participants.
2019
|
open-label proof-of-concept study |
4 |
↑Supports
|
The first four participants tolerated the 8-week MDMA-assisted psychotherapy course with no serious MDMA-related adverse events and no unexpected physiological, blood, or ECG changes; drinking outcomes were not yet reported. |
|
MDMA-assisted PTSD and Alcohol Therapy Trial (MPATHY): study protocol for a double-blind, randomised, controlled outpatient trial of MDMA-assisted integrated exposure-based therapy for comorbid post-traumatic stress disorder and alcohol use disorder
2026
|
RCT protocol |
100 |
?Unclear
|
Describes a planned double-blind trial comparing MDMA-assisted integrated exposure therapy with active-control (niacin)-assisted therapy on PTSD symptoms and heavy drinking days; no outcome data yet. |
|
Why MDMA therapy for alcohol use disorder? And why now?
2018
|
theoretical paper |
|
↑Supports
|
Argues that MDMA-assisted psychotherapy may suit alcohol use disorder because MDMA lets patients explore painful memories without being overwhelmed, and notes it had not been formally studied for substance use disorders. |
|
Psilocybin and MDMA in Couples Therapy: Investigating Treatment for Substance Use Disorders and Codependency
2025
|
narrative review |
|
↑Supports
|
Proposes that combining psilocybin-assisted therapy for substance use disorder with MDMA for a partner's codependency in couples therapy may reduce addictive and codependent behaviors. |
|
Efficacy and Safety of Psychedelics in Mental Disorder Cases: An Umbrella Review of Meta-Analyses of Randomized Controlled Trials
2025
|
umbrella review of meta-analyses of RCTs |
|
↕Mixed
|
Finds strong evidence for psilocybin in depression and MDMA in PTSD, but far fewer meta-analyses for substance use indications (e.g., LSD in alcohol use disorder), and flags methodological limitations and gaps in long-term safety data. |
|
Persisting Reductions in Cannabis, Opioid, and Stimulant Misuse After Naturalistic Psychedelic Use: An Online Survey
2020
|
cross-sectional online survey |
|
↑Supports
|
Reports that naturalistic psychedelic use is associated with self-reported persisting reductions in cannabis, opioid, and stimulant misuse, while noting the design cannot establish causality. |
|
User perceptions of the benefits and harms of hallucinogenic drug use: A web-based questionnaire study
2010
|
cross-sectional web survey |
600 |
↑Supports
|
Users reported benefits including help with addictions and mood disorders, and reported less harm from classic hallucinogens than from MDMA, cannabis, ketamine, and alcohol. |
|
Ecstasy (MDMA) dependence
1999
|
case series |
3 |
↓Opposes
|
Describes three cases meeting dependence criteria, arguing MDMA can be addictive in rare cases and that very heavy use may cause lasting neuronal changes; one case was linked to self-medication of PTSD. |
|
Test–re‐test reliability of DSM‐IV adopted criteria for 3,4‐methylenedioxymethamphetamine (MDMA) abuse and dependence: a cross‐national study
2009
|
test-retest diagnostic study |
593 |
↓Opposes
|
At baseline 15% met MDMA abuse and 59% met dependence criteria, with moderate test-retest reliability (kappa 0.69) and withdrawal among the most prevalent criteria. |
|
Self-reported prevalence of dependence of MDMA compared to cocaine, mephedrone and ketamine among a sample of recreational poly-drug users
2014
|
cross-sectional survey |
|
↓Opposes
|
MDMA users were more likely to report three or more DSM-IV dependence symptoms than users of cocaine, mephedrone, or ketamine, yet less likely to want to use less or seek help. |
|
Adverse events associated with classic psychedelics and MDMA: a real-world population-based study using the WHO pharmacovigilance database (VigiBase)
2025
|
pharmacovigilance database analysis |
|
↓Opposes
|
MDMA reports were associated with significantly greater odds of reported alcohol abuse, substance use disorder, and substance dependence than acetaminophen and oxycodone controls. |
|
Reinforcing Effects of MDMA (‘Ecstasy’) in Drug-Naive and Cocaine-Trained Rats
2001
|
animal experimental study |
|
↓Opposes
|
Intravenous MDMA was self-administered with equal reinforcing effect in drug-naive and cocaine-trained rats, and MDMA and cocaine produced distinct interoceptive stimuli. |
|
Use and abuse of dissociative and psychedelic drugs in adolescence
2021
|
review |
|
?Unclear
|
Notes that little is known about MDMA effects in adolescents and that MDMA produces mixed reinforcing and aversive effects whose balance may differ between adolescents and adults. |
|
Potential Human Neurotoxicity of MDMA (‘Ecstasy’): Subjective Self-Reports, Evidence from an Italian Drug Addiction Centre and Clinical Case Studies
2000
|
review and clinical case series |
|
↓Opposes
|
Reports that longer-term, larger-dose MDMA consumers were at high risk of psychopathological disturbances including depression, psychotic disorders, and cognitive problems, while noting MDMA was rarely the only drug used. |
|
Neural Correlates of the Severity of Cocaine, Heroin, Alcohol, MDMA and Cannabis Use in Polysubstance Abusers: A Resting-PET Brain Metabolism Study
2012
|
cross-sectional PET imaging study |
49 |
↓Opposes
|
Severity of MDMA use correlated negatively with brain metabolism in dorsolateral prefrontal and temporal cortex, controlling for other drugs used. |
|
Methamphetamine and MDMA (Ecstasy) Neurotoxicity: 'of Mice and Men'
2004
|
review |
|
↓Opposes
|
Argues that rodent and primate evidence indicates MDMA and methamphetamine cause neurotoxicity in dopaminergic and serotonergic neurons, while human data remain limited. |