Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2018 Dec;32(12):1295-1307.
doi: 10.1177/0269881118806297. Epub 2018 Oct 29.

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

Affiliations
Clinical Trial

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

Marcela Ot'alora G et al. J Psychopharmacol. 2018 Dec.

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.

Keywords: 3,4-Methylenedioxymethamphetamine (MDMA); depression; oxytocin; posttraumatic stress disorder; serotonin; sleep disturbance.

PubMed Disclaimer

Conflict of interest statement

Declaration of conflicting interests: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: M Ot’alora G received research funds from MAPS Public Benefit Corporation (MPBC) as the clinical trial principal investigator as well as for training and supervision of research psychotherapists. J Grigsby received research funds from MPBC as a clinical trial sub-investigator. B Poulter received research funds from MPBC as a clinical trial sub-investigator and as study administrator. JW Van Derveer III received research funds from MPBC as a clinical trial sub-investigator and as a study physician. SG Giron received research funds from MPBC as a clinical trial sub-investigator and from MAPS for directing the Zendo Project. S Hamilton received research funds from MPBC as a biostatistician. A Feduccia, A Emerson and L Jerome received salary support for full-time employment with MPBC. B Yazar-Klosinski and R Doblin received salary support for full-time employment with MAPS. M Mithoefer received research funds from MPBC as clinical trial medical monitor as well as for training of research psychotherapists.

Figures

Figure 1.
Figure 1.
Consolidated Standards of Reporting Trials (CONSORT) diagram.
Figure 2.
Figure 2.
Study design. BDI-II: Beck Depression Inventory-II; CAPS-IV: Clinician Administered PTSD Scale; DES-II: Dissociative Experience Scale-II; EKG: electrocardiogram; MDMA: 3,4-methylenedioxymethamphetamine; PSQI: Pittsburgh Sleep Quality Index; PTSD: posttraumatic stress disorder; SCID: Structured Clinical Interview for Diagnoses Axis I Research Version.
Figure 3.
Figure 3.
Change over time in Clinician Administered PTSD Scale (CAPS-IV) total scores in the intent-to-treat set. The primary endpoint occurred one month after the second blinded 3,4-methylenedioxymethamphetamine (MDMA) session. After assessment, the blind was broken. The active dose groups (100 and 125 mg) had one additional open-label MDMA session and completed an assessment two months after the third session. The comparator group (40 mg) crossed over to receive three open-label (100–125 mg) sessions, with assessments after the second and third sessions. The 12-month follow-up visit occurred after the final open-label MDMA session. PTSD: posttraumatic stress disorder; SD: standard deviation.

References

    1. Baggott MJ, Coyle JR, Siegrist JD, et al. (2016) Effects of 3,4-methylenedioxymethamphetamine on socioemotional feelings, authenticity, and autobiographical disclosure in healthy volunteers in a controlled setting. J Psychopharmacol 30: 378–387. - PubMed
    1. Baggott MJ, Kirkpatrick MG, Bedi G, et al. (2015) Intimate insight: MDMA changes how people talk about significant others. J Psychopharmacol 29: 669–677. - PMC - PubMed
    1. Beck AT, Steer RA. (1984) Internal consistencies of the original and revised Beck Depression Inventory. J Clin Psychol 40: 1365–1367. - PubMed
    1. Beck AT, Steer RA, Ball R, et al. (1996) Comparison of Beck Depression Inventories -IA and -II in psychiatric outpatients. J Pers Assess 67: 588–597. - PubMed
    1. Bedi G, Cecchi GA, Slezak DF, et al. (2014) A window into the intoxicated mind? Speech as an index of psychoactive drug effects. Neuropsychopharmacology 39: 2340–2348. - PMC - PubMed

Publication types

MeSH terms

Substances