Trials / Completed
CompletedNCT04280965
Quetiapine Augmentation of PE Therapy for the Treatment of Co-occurring PTSD and Mild Traumatic Brain Injury
Quetiapine Augmentation of Prolonged Exposure (PE) Therapy for the Treatment of Co-occurring PTSD and Mild Traumatic Brain Injury
- Status
- Completed
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 28 (actual)
- Sponsor
- The University of Texas Health Science Center at San Antonio · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A pilot study to evaluate feasibility for a full-scale merit application. Specifically, for veterans considering prolonged exposure (PE) therapy, following the model established by Foa et al, we need to establish safety, and feasibility of quetiapine compared to treatment as usual (TAU) which employs multiple medications commonly used for PTSD in the VA system.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Quetiapine Fumarate | Atypical antipsychotic |
| OTHER | Standard of care meducations | SSRI's/SNRI's/Trazodone/Prazosin/Hydroxyzine |
Timeline
- Start date
- 2019-02-01
- Primary completion
- 2022-04-29
- Completion
- 2022-10-17
- First posted
- 2020-02-21
- Last updated
- 2023-05-09
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04280965. Inclusion in this directory is not an endorsement.