Could a party drug ease PTSD?
NCT ID NCT06215261
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a drug called methylone in 62 adults with severe PTSD. Participants took methylone capsules once a week for 3 to 4 weeks. Researchers measured changes in PTSD and depression symptoms to see if the drug is safe and helpful.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- methylone
- What this could lead to
- If it works, this could point toward a new treatment option for people with PTSD.
- What could go wrong
- This is a small, early-phase trial with only 62 participants. It may not work for everyone, and side effects are possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
62 people
The number who actually took part.
- Started
-
Apr 2024
- Finished
-
Sep 2025
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 70 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Meets DSM-5 criteria for severe PTSD diagnosis, with a symptom duration of at least 6 months. * Tried at least one treatment for PTSD (either psychotherapy or pharmacological treatment). * Proficient in reading and writing in local language sufficient to complete questionnaires. * Free from any other clinically significant illness or disease. Exclusion Criteria: * Primary diagnosis of any other DSM-5 disorder. * Body mass index (BMI) \<18kg/m2 or ≥40 kg/m2. * Smokes an average of \>10 cigarettes and/or e-cigarettes per day. * Uncontrolled hypertension at Screening. * Use of prohibited concomitant medications or therapies. * Current or previous history of clinically significant cardiovascular/cerebrovascular conditions.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Post traumatic stress disorder are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Accel Research
Maitland, Florida, 32751, United States
-
CNS Healthcare
Orlando, Florida, 32801, United States
-
Clerkenwell Health
London, United Kingdom
-
Monarch Mental Health Group
Melbourne, Victoria, Australia
-
Numinus
Draper, Utah, 84020, United States
-
Ramsay Clinic Albert Road
Melbourne, Victoria, 3004, Australia
-
Redbird Research LLC
Las Vegas, Nevada, 89119, United States
-
Seattle NTC
Bellevue, Washington, 98004, United States
-
Segal Trials
Lauderhill, Florida, 33319, United States
-
Sunstone Medical
Rockville, Maryland, 20850, United States
-
Swinburne University of Technology
Hawthorn, Victoria, 3122, Australia
-
Uptown Clinical Research
Chicago, Illinois, 60640, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Five sessions to quiet trauma nightmares in bipolar disorder
- Can training hospital staff in Trauma-Informed care make childbirth safer?
- Scientists probe brain's reward system in mental illness
- Can a mindfulness class help veterans with concussion and PTSD?
- Can MDMA plus therapy help veterans fight both PTSD and alcohol addiction?
- Can talk therapies quiet the trauma of violence?