Overview

Iloperidone for Symptoms of Arousal in Post Traumatic Stress Disorder (PTSD)

Status:
Terminated
Trial end date:
2014-02-01
Target enrollment:
0
Participant gender:
All
Summary
A Double-Blind Placebo-Controlled Random Order Crossover Pilot Study of Iloperidone for Symptoms of Arousal in PTSD.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Colorado, Denver
Collaborator:
Novartis Pharmaceuticals
Treatments:
Iloperidone
Criteria
Inclusion Criteria:

- PTSD diagnosis

Exclusion Criteria:

- Pregnancy

- Traumatic Brain Injury greater than mild

- Primary sleep disorder

- Caffeinism

- Active substance use disorder

- Active suicidal risk

- Antipsychotic medication, antibiotics, sedatives, some antihypertensive or
antiarrhythmic medication