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ENROLLING BY INVITATION
NCT04216225

Pre-hospital Tourniquet in Extremity Injury

Sponsor: Methodist Health System

View on ClinicalTrials.gov

Summary

2.1. Objective: • Primary Objective: To compare outcomes of patients with extremity injuries presenting with or without pre-hospital tourniquet placement. 2.2. Study Outcome Measures * Primary Outcome: Incidence of arrival in shock (SBP \<90) * Secondary Outcomes: Demographics, comorbidities, mechanism of injury, cause of injury, diagnosis codes, procedure codes, Injury Severity Scale, Abbreviated Injury Scale, operative management vs. non-operative management, radiologic findings, pathologic findings, tourniquet effectiveness (as determined both subjectively by trauma surgeon and objectively by presence vs. absence of pulse below level of tourniquet application), total number of units of blood products transfused within first 24 hrs, total number of units of blood products for index admission, type of blood 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.

Official title: Prospective Observational Multi-center Analysis of Pre-hospital Tourniquet in Extremity Injury

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

150

Start Date

2018-11-01

Completion Date

2025-01-01

Last Updated

2024-11-20

Healthy Volunteers

No

Interventions

OTHER

pre-hospital tourniquet placement

patients with extremity injuries presenting with or without pre-hospital tourniquet placement.

Locations (1)

Methodist Dallas Medical Center

Dallas, Texas, United States