3,4-Methylenedioxymethamphetamine-assisted psychotherapy for treatment of chronic posttraumatic stress disorder: A randomized phase 2 controlled trial

Author:

Ot’alora G Marcela1,Grigsby Jim2,Poulter Bruce1,Van Derveer Joseph W3,Giron Sara Gael4,Jerome Lisa5ORCID,Feduccia Allison A5,Hamilton Scott6,Yazar-Klosinski Berra4,Emerson Amy5,Mithoefer Michael C7,Doblin Rick4

Affiliation:

1. Aguazul-Bluewater, Inc., Boulder, CO, USA

2. Department of Psychology, University of Colorado, Denver, CO, USA

3. Integrative Psychiatric Healing Center, Boulder, CO, USA

4. Multidisciplinary Association for Psychedelic Studies (MAPS), Boulder, USA

5. MAPS Public Benefit Corporation, Boulder, CO, USA

6. Stanford School of Medicine, Stanford, CA, USA

7. Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA

Abstract

Background: Posttraumatic stress disorder often does not resolve after conventional psychotherapies or pharmacotherapies. Pilot studies have reported that 3,4-methylenedioxymethamphetamine (MDMA) combined with psychotherapy reduces posttraumatic stress disorder symptoms. Aims: This pilot dose response trial assessed efficacy and safety of MDMA-assisted psychotherapy across multiple therapy teams. Methods: Twenty-eight people with chronic posttraumatic stress disorder were randomized in a double-blind dose response comparison of two active doses (100 and 125 mg) with a low dose (40 mg) of MDMA administered during eight-hour psychotherapy sessions. Change in the Clinician-Administered PTSD Scale total scores one month after two sessions of MDMA served as the primary outcome. Active dose groups had one additional open-label session; the low dose group crossed over for three open-label active dose sessions. A 12-month follow-up assessment occurred after the final MDMA session. Results: In the intent-to-treat set, the active groups had the largest reduction in Clinician-Administered PTSD Scale total scores at the primary endpoint, with mean (standard deviation) changes of −26.3 (29.5) for 125 mg, −24.4 (24.2) for 100 mg, and −11.5 (21.2) for 40 mg, though statistical significance was reached only in the per protocol set ( p=0.03). Posttraumatic stress disorder symptoms remained lower than baseline at 12-month follow-up ( p<0.001) with 76% ( n=25) not meeting posttraumatic stress disorder criteria. There were no drug-related serious adverse events, and the treatment was well-tolerated. Conclusions: Our findings support previous investigations of MDMA-assisted psychotherapy as an innovative, efficacious treatment for posttraumatic stress disorder.

Funder

Multidisciplinary Association for Psychedelic Studies

Publisher

SAGE Publications

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

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