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Evacuation Time and Tourniquet Use as Risk Factors for PTSD in Combat-Related Amputation

Study acronym: EVAC-PTSD Stud
StatusNot Yet Recruiting
PhaseNot specified
Started
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Record History

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  1. Study title shortened, about 4 wordsv2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study aims to evaluate the relationship between evacuation time, tourniquet use, and the development of post-traumatic stress disorder (PTSD) in patients with combat-related amputations. In the context of modern warfare, prolonged evacuation times and extended tourniquet application may contribute not only to physical injury but also to psychological trauma. The study will prospectively follow patients over 18 months to identify key predictors of PTSD and to assess their interaction.
Trial Details
NCT Number NCT07502313
Lead Sponsor Charitable Organisation Charitable Fund Superhumans (Co Cf Superhumans)
Conditions
(from sponsor)		 Amputation, PTSD, Combat Posttraumatic Stess Disorder, Combat Trauma
Related terms Stress Disorders, Post-Traumatic
Enrollment 300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov