CAP-Ketamine for Antidepressant Resistant PTSD
Completed · Phase 2 · Has a placebo group
Conditions studied: PTSD, Posttraumatic Stress Disorder
In brief
The purpose of this study is to test the safety and efficacy of repeated doses of ketamine as compared to placebo, in reducing symptoms of Posttraumatic Stress Disorder (PTSD) in an active duty military and Veteran population.
Key facts
- Study ID
- NCT02655692
- Run by
- VA Office of Research and Development
- People needed
- 163
- Starts
- 2016-04-18
- Expected to finish
- 2020-07-01
- Last updated by the study team
- 2022-06-02
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- male or female Veterans or active duty military personnel between the ages of 18 and 70 years
- diagnosis of PTSD
- history of trialing one or more antidepressant medications with little to no PTSD symptom improvement
- ability to provide written informed consent
You may not qualify if…
- females who are currently pregnant or breastfeeding
- current high risk for suicide
- history of severe head injury
Where it is running
- VA Connecticut Healthcare System West Haven Campus, West Haven, CT — West Haven, Connecticut, United States
- Minneapolis VA Health Care System, Minneapolis, MN — Minneapolis, Minnesota, United States
- Brooke Army Medical Center — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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