MDMA-Assisted Massed Exposure Therapy for PTSD

Part of paid clinical trials in Atlanta, Georgia.

Sponsor
Emory University
Study ID
NCT07288151
Phase
PHASE2
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
21 Years - 70 Years
Healthy Volunteers
Not accepted

Interventions

  • 3,4-Methylenedioxymethamphetamine (MDMA) — DRUG
    MDMA is a synthetic compound, commonly administered as MDMA hydrochloride (HCl). The drug will be administered in 100mg doses for a single session on Visit 2 out of 10- day study sessions over 2 weeks. MDMA is administered orally in capsule form and is taken under supervision in a controlled, therapeutic environment
  • Placebo — DRUG
    Placebos will visually match the 3 MDMA capsules (40mg, 40mg, and 20mg).
  • Massed Prolonged Exposure (PE) — BEHAVIORAL
    Massed exposure therapy will be conducted for 11 sessions, 10 daily sessions and an additional therapy session during V2. They will consist of repeated exposures to trauma memories (imaginal exposure) consistent with the manualized protocol for massed exposure therapy. Also consistent with this treatment manual, participants will listen to imaginal exposures outside of PE sessions for "homework."

Study Details

The goal of this clinical trial is to investigate the efficacy of 3,4-methylenedioxy-methamphetamine hydrochloride (MDMA) combined with Massed Prolonged Exposure (PE) therapy for the treatment of posttraumatic stress disorder (PTSD) in adult participants diagnosed with PTSD. This randomized, placebo-controlled trial will enroll 95 participants. The main questions it aims to answer are: * Does the combination of PE + MDMA lead to greater reduction in PTSD symptom severity from pre-treatment to one-month follow-up compared to PE + placebo? * Does PE + MDMA improve response efficiency and durability of PTSD symptom improvement compared to PE + placebo? * Does MDMA + PE enhance extinction retention and reduce amygdala threat reactivity, and are these changes associated with improved PTSD outcomes? Participants will: * Receive 10 sessions of Massed Prolonged Exposure therapy over two weeks * Be administered either 100 mg of MDMA or a placebo at Visit 2 * Undergo blinded independent evaluator assessments using the Clinician-Administered PTSD Scale for DSM-5-R (CAPS-5-R) at the one-month posttreatment follow-up

Key Dates

Start date
Jul 31, 2026
Status verified
May 2026
Primary completion
Jan 31, 2030
Completion
Jan 31, 2030

Study Design

Enrollment
200 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: MDMA group
  • Placebo Comparator: Standard of Care

Primary Outcome Measure

Changes in PTSD symptoms measured by CAPS-5-R [ Time Frame: Baseline, 1 month post-treatment ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Emory Brain Health CenterAtlantaGeorgia30329
Jessica Maples-Keller, PhD
404-712-1035

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