Vortioxetine for Posttraumatic Stress Disorder
Completed · Phase 4 · Has a placebo group
Conditions studied: Post-Traumatic Stress Disorder
In brief
Post-traumatic stress disorder (PTSD) can result from having experienced or witnessed a traumatic event. Patients with PTSD symptoms can sometimes experience symptom relief after treatment with antidepressants; however, few patients experience complete symptom relief. There is a need to develop new treatments for PTSD. This study will evaluate if 12 weeks of using Vortioxetine relieves PTSD symptoms. Vortioxetine has been approved for the treatment of depression; however, Vortioxetine has not been approved by the Food and Drug Administration for the treatment of PTSD.
Key facts
- Study ID
- NCT02637895
- Run by
- University of Miami
- People needed
- 41
- Starts
- 2016-12-01
- Expected to finish
- 2020-02-06
- Last updated by the study team
- 2021-02-08
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
Where it is running
- University of Miami — Miami, Florida, United States
- Emory University — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
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