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Completed

NCT Number: NCT00090064

MDMA-Assisted Psychotherapy in People With Posttraumatic Stress Disorder

The goal of this clinical trial is to compare MDMA-assisted therapy to placebo with therapy in people with chronic, treatment-resistant posttraumatic stress disorder (PTSD). The main question it aims to answer is: Is there a reduction in PTSD symptoms among people given MDMA-assisted therapy compared to placebo with therapy?

Participants will receive either MDMA-assisted therapy or placebo with therapy during two blinded experimental sessions spaced three to five weeks apart. During experimental sessions, participants receive an initial dose of 125 mg of MDMA HCl, or placebo, followed by a dose of 62.5 mg of MDMA HCl, or placebo. During this treatment period, participants will also undergo non-drug preparatory psychotherapy sessions and non-drug integrative sessions.

The study will test whether MDMA-assisted therapy can be safely given to participants. Researchers will compare PTSD symptoms in the MDMA-assisted therapy group to the placebo with therapy group to see if there is a reduction in symptoms after the treatment period.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Offices of Michael Mithoefer MD

Mt. Pleasant, South Carolina, 29464, United States

About this study

This randomized, double-blind placebo-controlled pilot study assessed the safety and effectiveness of MDMA-assisted therapy among people with chronic, treatment-resistant PTSD, including veterans. Participants were assigned to receive either MDMA-assisted therapy or placebo with therapy during two blinded experimental sessions spaced three to five weeks apart during Stage 1 of the study. During these experimental sessions, participants received an initial dose of 125 mg of MDMA HCl followed by a supplemental dose of 62.5 mg of MDMA HCl, or they received initial and supplemental doses of inactive placebo. Psychotherapists and independent raters were blinded to participants' treatment conditions. This treatment period also consisted of non-drug preparatory therapy sessions and non-drug integration therapy sessions.

During Stage 2 of the study, the blind was broken and participants assigned to receive MDMA-assisted therapy in Stage 1 underwent a third open-label experimental session of MDMA-assisted therapy. Participants assigned placebo with therapy during Stage 1 who chose to enroll in Stage 2 underwent three open-label sessions of MDMA-assisted therapy. Outcome measures were administered two months after the second experimental session in Stage 1 and four to six weeks after the second MDMA-assisted therapy session in Stage 2. A final data-collection session took place at two months after the third experimental session.

The primary objective of the study was to measure change in PTSD symptoms via CAPS-IV across the study in participants receiving MDMA-assisted therapy versus placebo with therapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have current PTSD (within the past 6 months) in response to crime victimization, including childhood sexual or physical abuse, or meet criteria for PTSD in response to combat;
  • Have a CAPS score showing moderate to severe PTSD symptoms;
  • They must either:
  • Have had at least one unsuccessful attempt at treatment for PTSD with a SSRI and psychotherapy;
  • Be a veteran with PTSD symptoms that have endured for no less than one year but no more than five years
  • Be at least 18 years old;
  • Must be generally healthy;
  • Willing to remain overnight at the study site;
  • Agree to have transportation home the morning after experimental sessions;
  • Are willing to be contacted via telephone for all necessary telephone contacts;
  • Must have a negative pregnancy test if able to bear children and agree to use an effective form of birth control;
  • Are proficient in reading English;

Exclusion criteria

  • Are pregnant or nursing, or are able to bear children and are not practicing an effective means of birth control;
  • Weigh less than 50 kg or more than 105 kg;
  • Are unable to give adequate informed consent;
  • Prior use of "Ecstasy" (illicit drug preparations purported to contain MDMA) more than 5 times or at any time within the previous 6 months;
  • Have a history of certain excluded medical disorders.

Treatment and study plan

Midomafetamine HCl

Drug

125 mg of midomafetamine HCl followed by a supplemental half-dose of 62.5 mg of midomafetamine HCl

Other names: MDMA HCl, 3,4-methylenedioxymethamphetamine, MDMA, Midomafetamine

Lactose placebo pill

Drug

125 mg followed by a supplemental half-dose of 62.5 mg

Other names: Placebo

Therapy

Behavioral

Non-directive therapy provided by a team of two co-therapists

Primary outcomes

  1. Change in Clinician-Administered PTSD Scale (CAPS-IV) From Baseline to 2-month Follow-up

    Time frame: Baseline to 2 months post second experimental session

    The Clinician-Administered PTSD Scale for DSM-IV (CAPS-IV) is a clinician administered and scored assessment of PTSD symptoms via structured interview based upon PTSD diagnosis in DSM-IV. The total severity score is a sum of symptom frequency and intensity scores for the subscales B (re-experiencing), C (avoidance) and D (hypervigilance) and ranges from 0 to 136, with higher scores indicating greater severity of PTSD symptoms.

Secondary outcomes

  1. Change in Impact of Events Scale Revised (IES-R) From Baseline to 2-month Follow-up

    Time frame: Baseline to 2 months post second experimental session

    The Impact of Events Scale Revised (IES-R) is a 22-item self-report measure (for DSM-IV) designed to measure the extent to which a given stressful life event produces subjective distress. Each item corresponds directly to 14 of the 17 DSM-IV symptoms of PTSD and is rated on a 5-point scale ranging from 0 ("not at all") to 4 ("extremely") for the extent to which the item was true for the participant during the past seven days. The IES-R yields a total score ranging from 0 to 88 with higher scores indicated greater distress.

Sponsors and collaborators

Lead sponsor

Resilient Pharmaceuticals

Industry

Registry information

Official study title

Phase II Clinical Trial Testing the Safety and Efficacy of 3,4-Methylenedioxymethamphetamine (MDMA)-Assisted Psychotherapy in Subjects With Chronic Posttraumatic Stress Disorder

Important dates

Study start
2004
Primary completion
2008
Study completion
2010
First posted
Aug 25, 2004
Registry last updated
Jun 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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