RecruitingNot ApplicableNCT02880163

REVIVE: Reducing Exsanguination Via In-Vivo Expandable Foam

Reducing Exsanguination Via In-Vivo Expandable Foam


Sponsor

Arsenal Medical, Inc.

Enrollment

40 participants

Start Date

Aug 7, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to demonstrate safety, effectiveness and benefit-risk profile of ResQFoam for the inhospital treatment of exsanguinating, intraabdominal haemorrhage due to trauma in patients where emergent laparotomy is required.


Eligibility

Min Age: 15 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called ResQFoam for people with exsanguinating hemorrhage, hemorrhagic shock, and other related conditions. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 15 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEResQFoam

Hemostatic device for the treatment of emergent, exsanguinating, Class III or IV intraabdominal hemorrhagic shock in subjects due to trauma


Locations(2)

University of Alabama at Birmingham

Birmingham, Alabama, United States

University of Cincinnati

Cincinnati, Ohio, United States

View Full Details on ClinicalTrials.gov

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NCT02880163


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