Pre-hospital Tourniquet in Extremity Injury
-
- STATUS
- Recruiting
-
- participants needed
- 150
-
- sponsor
- Methodist Health System
Summary
2.1. Objective:
Primary Objective: To compare outcomes of patients with extremity
2.2. Study Outcome Measures
- Primary Outcome: Incidence of arrival in
shock (SBP <90) - Secondary Outcomes: Demographics, comorbidities, mechanism of
injury , cause ofinjury , diagnosis codes, procedure codes, ISS, AIS, operative management vs. non-operative management, radiologic findings, pathologic findings, tourniquet effectiveness (as determined both subjectively bytrauma surgeon and objectively by presence vs. absence of pulse below level of tourniquet application), total number of units ofblood products transfused within first 24 hrs, total number of units ofblood products for index admission, type ofblood products or other fluid given, hospital length of stay, ICU length of stay, ventilator days,infectious complications, other complications, discharge disposition, 24 hr mortality, overall mortality.
Description
This is a prospective, observational study. All patients who present to the participating
ED's who meet inclusion/exclusion criteria will be identified by the treating
Details
| Condition |
Extremity |
|---|---|
| Age | 18years - 100years |
| Treatment | pre-hospital tourniquet placement |
| Clinical Study Identifier | NCT04216225 |
| Sponsor | Methodist Health System |
| Last Modified on | 19 February 2024 |
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