Feasibility of Evaluating XSTAT Use in the Prehospital Setting

Stopped early · Not applicable

Conditions studied: Shock, Hemorrhagic, Injury Penetrating, Hemorrhage

In brief

This study evaluates the prehospital use of the XSTAT device to control bleeding in junctional wounds. Participants will be randomized to the use of XSTAT versus standard care.

Key facts

Study ID

NCT04663087

Run by

University of Alabama at Birmingham

People needed

1

Starts

2022-10-29

Expected to finish

2023-08-11

Last updated by the study team

2024-12-30

Who can join

Age: 15 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥15 years or estimated body weight ≥50 kg.
• Penetrating junctional injury (femoral or axillary), with i. visible bleeding ii. too proximal to be controlled with a tourniquet
• Patient will be taken to participating level I trauma center, directly from the scene

You may not qualify if…

• Prisoners, children <15 years old, known pregnant patients.
• Patients receiving chest compressions (prior to XSTAT® use).
• Patients with an opt-out bracelet.

Where it is running

• UAB Hospital — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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