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Survey of Tourniquet Use in a Combat Support Hospital

Survey of Tourniquet Use in a Combat Support Hospital

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00517166
Enrollment
584
Registered
2007-08-16
Start date
2006-08-31
Completion date
2008-03-31
Last updated
2011-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vascular Injury

Keywords

tourniquet, extremity injury, hemostatic device

Brief 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.

Detailed description

This is a performance improvement project that is a prospective observational cohort design with subgroup analyses. This project meets the criteria of research with its intent to publish. No data is generated and only existing data are used. No interventions are made and the comparisons will be with within subgroups in the cohort. Aim 1. Describe the number of tourniquets which were appropriately used (wound required a tourniquet and tourniquet was placed properly) as assessed by treating physician Aim 2 &3. Describe if limbs wounds with tourniquets were bleeding upon admission, resuscitation, and following tourniquet removal Aim 4. Describe if mortality for the cohort of patients with tourniquets is different than the mortality predicted by various injury scoring systems Aim 5. Compare patient outcomes between those in which a tourniquet was indicated but not used and those for whom a tourniquet was indicated and used Aim 6. Determine if patients that received tourniquets for an extended time period exhibit any known tourniquet complications

Interventions

DEVICECAT (Combat Arms Tourniquet)

device

Sponsors

United States Army Institute of Surgical Research
Lead SponsorFED

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* penetrating extremity injury with tourniquet use

Exclusion criteria

* non penetrating extremity injury

Countries

Iraq

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026