Effects of Stimulant Medications in PTSD
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- University of Chicago
- Study ID
- NCT07664631
- Phase
- PHASE1
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Placebo — DRUGdextrose
- Adderall — DRUGmixed amphetamine salts
Study Details
While there have been advances in understanding post-traumatic stress disorder (PTSD) as a disorder and its biological features, unfortunately only one out of five traumatized persons with PTSD reach remission after cycling through evidence-based and/or FDA-approved medications. This is especially unfortunate given that people with PTSD are often from vulnerable populations, or those whose professions entail personal sacrifice. It is clear that new serotonergic antidepressants and atypical antipsychotics will not be sufficient to fix this gap, and new mechanisms of action need to be tested. In the current proposal, the investigators test the hypothesis that mixed amphetamine salts (brand name Adderall), FDA-approved for treating attention deficit hyperactivity disorder (ADHD), can improve PTSD outcomes.
Key Dates
- Start date
- Sep 15, 2026
- Status verified
- Jun 2026
- Primary completion
- Sep 15, 2027
- Completion
- Sep 15, 2027
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- TREATMENT
Arms
- Placebo Comparator: placebodextrose
- Experimental: AdderallAdderall (20 mg)
Primary Outcome Measure
Quality of Social Interaction Ratings using the Conversation Questionnaire [ Time Frame: Completed 4 hours post-drug administration during both sessions (drug, placebo) ]
Central Contacts
- Hanna Molla7737023560
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Chicago | Chicago | Illinois | 60637 | Royce Lee (PRINCIPAL_INVESTIGATOR) |
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