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NCT02880163 · ClinicalTrials.gov registry record · NA
REVIVE: Reducing Exsanguination Via In-Vivo Expandable Foam
A NA study of Trauma and Hemorrhagic Shock, sponsored by Arsenal Medical.
- Recruiting
- Registry status
- NA
- Development phase
- 40
- Enrollment target
- 2
- Study locations
NCT02880163 is a NA study of Trauma and Hemorrhagic Shock that is actively recruiting participants, run by Arsenal Medical. The registered enrollment target is 40 participants, below the 307-participant average among 56 other Trauma trials with a reported enrollment target (87% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT02880163, a NA study of Trauma and Hemorrhagic Shock, is actively recruiting participants, sponsored by Arsenal Medical.
- RECRUITING
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
- 2
- Study locations
Study 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.
Conditions Studied
Interventions
- DEVICE ResQFoam
Study Locations (2)
Alabama
- University of Alabama at Birmingham - Birmingham
Ohio
- University of Cincinnati - Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2025-08-07 |
| Est. Completion | 2026-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02880163
The ClinicalTrials.gov registry entry for NCT02880163 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 307-participant average among 56 other Trauma trials with a reported enrollment target (87% lower). The listed sponsor is Arsenal Medical, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Trauma appearing as the primary indexed condition, and to 1 intervention - of which ResQFoam is the first listed.
NCT02880163 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Alabama, Ohio.
Frequently Asked Questions
What is clinical trial NCT02880163 about?
NCT02880163 is a clinical study titled "REVIVE: Reducing Exsanguination Via In-Vivo Expandable Foam". 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.
What is the current status of trial NCT02880163?
This trial is currently recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2025-08-07. Estimated completion is 2026-12-31.
What conditions does trial NCT02880163 study?
This clinical trial studies the following conditions: Trauma, Hemorrhagic Shock, Exsanguinating Hemorrhage, Shock; Traumatic.
What interventions are being tested in trial NCT02880163?
The interventions under investigation include: ResQFoam (DEVICE).
Who is sponsoring clinical trial NCT02880163?
This trial is sponsored by Arsenal Medical, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02880163 being conducted?
This trial has 2 study locations across Alabama, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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