Survey of Tourniquet Use in a Combat Support Hospital

NCT00517166 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 584

Last updated 2011-12-20

No results posted yet for this study

Summary

Data will be collected on the type of tourniquet and circumstances of its use. Patients with penetrating extremity injury will have clinical and pre-clinical hospital data collected.

Conditions

  • Vascular Injury

Interventions

DEVICE

CAT (Combat Arms Tourniquet)

device

Sponsors & Collaborators

  • United States Army Institute of Surgical Research

    lead FED

Principal Investigators

  • John F Kragh, MD · US Army Institute of Surgical Research

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-08-31
Completion
2008-03-31

Countries

  • Iraq

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00517166 on ClinicalTrials.gov