MDMA-assisted psychotherapy for the treatment of PTSD: A systematic review and meta-analysis of randomized controlled trials (RCTs).

Journal: Neuropsychopharmacology reports

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Affiliated Institutions:  Department of Community and Mental Health Nursing, Faculty of Nursing, Jordan University of Science and Technology, Irbid, Jordan. Department of Psychiatry, Jinnah Sindh Medical University, Karachi, Pakistan. Department of Psychiatry, University of Tripoli, Tripoli, Libya. Department of Psychiatry, Karachi Medical and Dental College, Karachi, Pakistan. Department of Psychiatry, Allama Iqbal Medical College, Lahore, Pakistan. Department of Psychiatry, Rawalpindi Medical College, Rawalpindi, Pakistan. Department of Psychiatry, CMH Lahore Medical College, Lahore, Pakistan. Department of Psychiatry, Khyber Medical University, Peshawar, Pakistan. Avalon University School of Medicine, Willemstad, Curaçao. Department of Psychiatry, King Edward Medical University, Lahore, Pakistan. Hamad Medical Corporation, Doha, Qatar.

Abstract summary 

Post-traumatic stress disorder (PTSD) is a mental health disorder resulting from exposure to traumatic events, manifesting in various debilitating symptoms. Despite available treatments, many individuals experience inadequate response or significant side effects. Previous reviews suggest promising outcomes with MDMA-assisted psychotherapy (MDMA-AT), but limitations prompt the need for a comprehensive evaluation.We searched various online databases and registries such as MEDLINE (via PubMed), Embase, the Cochrane Central Register of Controlled Trials (CENTRAL), and ClinicalTrials.gov to retrieve RCTs that fit our inclusion criteria. We performed meta-analyses using Review Manager by applying a random-effects model. Dichotomous and continuous outcomes were pooled as risk ratios (RR) and standard mean difference (SMD), respectively.Nine studies with a total of 297 participants with PTSD were included in our meta-analysis. The control group consisted of inactive doses of MDMA (25-40 mg) or placebo. Our meta-analysis showed that MDMA-AT led to a significant reduction in the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) severity scores as compared to the control group (SMD -1.10, 95% CI: -1.62 to -0.59). More patients in the MDMA-AT group exhibited significant response (RR 1.59, 95% CI: 1.22, 2.08) and remission (RR 2.32, 95% CI: 1.47 to 3.66) as compared to patients in the control group. There was no significant difference regarding the incidence of ≥1 treatment-emergent adverse events (TEAE), ≥1 severe TEAE, and suicidal ideation between the two groups.MDMA-AT demonstrates significant efficacy in improving PTSD symptoms, enhancing both response and remission rates in individuals with chronic, treatment-resistant PTSD, while maintaining a favorable safety profile.

Authors & Co-authors:  Shahrour Ghada G Sohail Kainat K Elrais Safa S Khan Muhammad Hamza MH Javeid Javeria J Samdani Khubaib K Mansoor Hajra H Hussain Syed Izhar SI Sharma Dhruvikumari D Ehsan Muhammad M Nashwan Abdulqadir J AJ

Study Outcome 

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Citations :  Sherin JE, Nemeroff CB. Post‐traumatic stress disorder: the neurobiological impact of psychological trauma. Dialogues Clin Neurosci. 2011;13(3):263–278. https://doi.org/10.31887/DCNS.2011.13.2/jsherin
Authors :  11
Identifiers
Doi : 10.1002/npr2.12485
SSN : 2574-173X
Study Population
Male,Female
Mesh Terms
Other Terms
MDMA‐AT;RCTs;meta‐analysis;post‐traumatic stress disorder
Study Design
Randomized Control Trial
Study Approach
Systemic Review
Country of Study
Publication Country
United States