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Utility and Procedural Feasibility of REBOA Operationalized for Non-Trauma Application (UP-FRONT) — UP-FRONT  

Ventricular Tachycardia Clinical Trial

Official title:
Utility and Procedural Feasibility of REBOA Operationalized for Non-Trauma Application (UP-FRONT)

Clinical Trial Summary

Single center randomized-controlled trial in out-of-hospital cardiac arrest (OHCA) patients. This study will investigate the feasibility and utility of the Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) procedure using a REBOA catheter device in patients who have experienced an OHCA and have not regained return of spontaneous circulation (ROSC).

Clinical Trial Description

Victims arriving to, or experiencing witnessed Ventricular Fibrillation (VF) or Ventricular Tachycardia (VT) out of hospital cardiac arrest in, the UAB emergency department with greater than 10 minutes of conventional ACLS will be eligible. The study population will consist of forty (40) subjects randomized to either continued contemporary standard of care (ACLS), or ACLS plus the administration of a REBOA catheter device. The aims of UPFRONT are: 1. To describe the feasibility of rapid deployment of a REBOA catheter device in the setting of OHCA 2. To evaluate the utility of a REBOA catheter device to achieve ROSC in the setting of OHCA. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05236920
Study type Interventional
Source University of Alabama at Birmingham
Contact
Status Withdrawn
Phase N/A
Start date October 1, 2022
Completion date October 31, 2022
View Details
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