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Not Yet RecruitingNCT07502313

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

Evacuation Time and Tourniquet Use as Risk Factors for PTSD in Combat-Related Amputation: A Prospective Cohort Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
Charitable Organisation Charitable Fund Superhumans (Co Cf Superhumans) · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

Combat-related amputations are frequently associated with prolonged evacuation times and the use of hemostatic tourniquets. While these factors are critical for survival, their potential contribution to long-term psychological outcomes remains insufficiently studied. This prospective longitudinal study will investigate how evacuation delays and tourniquet duration influence the development of PTSD symptoms in Ukrainian veterans with limb amputations. The study will also evaluate the interaction between these factors and their cumulative psychological impact. Participants will be followed for 18 months using validated PTSD screening tools, including the PCL-5 questionnaire, combined with retrospective analysis of medical records.

Conditions

Timeline

Start date
2026-03-15
Primary completion
2026-11-15
Completion
2026-11-15
First posted
2026-03-30
Last updated
2026-04-03

Locations

1 site across 1 country: Ukraine

Source: ClinicalTrials.gov record NCT07502313. Inclusion in this directory is not an endorsement.