PTSDSafety & Risk ManagementSet & SettingMDMA

Side-effects of mdma-assisted psychotherapy: a systematic review and meta-analysis

This systematic review and meta-analysis (2024) examined the side effects of MDMA-assisted psychotherapy (MDMA-AP) across Phase II and III studies. Thirteen studies were included, with most showing an increase in side effects during medication sessions and the following week compared to control conditions. Despite these findings, the overall certainty of evidence was rated as very low to moderate, and the quality of side effects reporting was generally poor, suggesting further research is needed to fully understand the safety profile of MDMA-AP.

Authors

  • Gillinder Bedi
  • Olivia Carter

Published

Neuropsychopharmacology
meta Study

Abstract

Evidence suggests that MDMA-assisted psychotherapy (MDMA-AP) has therapeutic potential for treatment of psychiatric illness. We conducted the first comprehensive systematic review and meta-analysis of the side effects of MDMA-AP across indications. We also assessed the quality of side effects-reporting in published trials of MDMA-AP. PubMed, EMBASE, PsycINFO, MEDLINE and Cochrane Central Register of Controlled Trials (CENTRAL) were systematically searched. Phase 2 and 3 MDMA-AP studies were included; Phase 1 studies, which assessed MDMA without psychotherapy, were not. Quality of side effects-reporting was assessed against the CONSORT Harms 2022 guidelines. We also compared numbers of adverse events reported in publications to those recorded in ClinicalTrial.gov registers. Thirteen studies were included, with eight contributing to the meta-analysis. In Phase 2 studies, MDMA-AP was associated with increased odds of any side effect during medication sessions (OR = 1.67, 95%CI (1.12, 2.49)) and in the 7 days following (OR = 1.59, 95%CI (1.12, 2.24)) relative to control conditions. In Phase 3 studies, MDMA-AP was associated with increased odds of any adverse event during the treatment period relative to placebo-assisted psychotherapy (OR = 3.51, 95%CI (2.76, 4.46)). The majority of RCTs were rated as having high risk of bias. Certainty of the evidence was rated as very low to moderate according to the GRADE framework. No included RCT had adequate adherence to the CONSORT Harms 2022 recommendations and reporting rates were also low. Compared to placebo, MDMA-AP was associated with increased odds of side effects, which were largely transient and mild or moderate in severity. However, identified limitations in existing evidence indicate that further investigation is needed to better characterize the safety profile of MDMA-AP and guide implementation.

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Research Summary of 'Side-effects of mdma-assisted psychotherapy: a systematic review and meta-analysis'

Introduction

Colcott and colleagues place MDMA-assisted psychotherapy (MDMA-AP) in the context of a rapidly advancing clinical literature, noting that the intervention combines pharmacotherapy and psychotherapy in protocols that typically include preparatory sessions, two to three full-day MDMA- or placebo-assisted sessions, and subsequent integration sessions. Earlier trials and reviews have suggested therapeutic potential for post‑traumatic stress disorder (PTSD) and possibly other conditions, and recent regulatory moves (for example, a TGA decision in Australia and an anticipated FDA approval) have increased interest in wider clinical use. At the same time, the authors highlight concerns about potential harms unique to combining a psychoactive drug with psychotherapy and about inconsistent or inadequate adverse-event assessment and reporting in existing trials. This paper therefore aimed to provide the first comprehensive, across‑indications systematic review and meta-analysis of side effects in Phase II and III trials of MDMA-AP. In addition to estimating pooled risks for a range of safety outcomes, the investigators assessed the quality of harms reporting in published randomized controlled trials against the CONSORT Harms 2022 guideline and compared adverse events reported in publications with those recorded on ClinicalTrials.gov. The term "side effects" is used broadly to encompass spontaneous reactions, treatment‑emergent adverse events (TEAEs) and other harms as reported in the source trials.

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Study Details

References (19)

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