A Phase 4 study on the effect of ketamine and etomidate during RSI on long-term outcomes
Recruiting by Invitation NCT06179485
Study Description
Evaluating the impact of ketamine and etomidate on reducing post-traumatic stress disorder (PTSD) after critical illness and intubation
Study Details
- Registry ID:
- NCT06179485
- Conditions:
- Post-Traumatic Stress Disorder, Acute Respiratory Failure
- Phase:
- Target Enrollment:
- 1,756 participants
- Start Date:
- Healthy Volunteers:
- No
Study Locations (6 sites)
-
Wake Forest Baptist Medical Center
Winston-Salem, North Carolina, United States -
University of Alabama Hospital
Birmingham, Alabama, United States -
Vanderbilt University Medical Center
Nashville, Tennessee, United States -
Hennepin County Medical Center
Minneapolis, Minnesota, United States -
University of Colorado Denver
Aurora, Colorado, United States -
Denver Health Medical Center
Denver, Colorado, United States
Interested in Participating?
Check your eligibility and learn more about this study on TrialScreen.