4491903
Last Update Posted: 2021-05-04
Recruiting has ended
All Genders accepted | 18 Years-65 Years |
0 Estimated Participants | No Expanded Access |
Interventional Study | Does not accept healthy volunteers |
REBOA for Out-of-hospital Cardiac Arrest
Cardiac arrest is a major health problem that carries a high mortality rate. Substantial research and development have been put into changing the outcome of cardiac arrest and despite the advent of automated external defibrillators (AED), increase in bystander Cardiopulmonary resuscitation (CPR) and automated CPR devices (ACPR), the proportion of patient survival to hospital discharge has only minimally improved.
The objective is to investigate safety and performance of the Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) procedure as an adjunct to Advanced Life Support (ALS) for treatment of refractory cardiac arrest.
The scope of the study is to collect data on patients with refractory out of hospital cardiac arrest (OHCA) for this feasibility study.
Data collected:
- from enrolment of the patient until hospital arrival
- every 24 hours
- at discharge or 7 days post enrollment
- at 30 days post enrollment
The investigation is initiated to investigate the safety and performance of the REBOA procedure for patients experiencing refractory OHCA.
Eligibility
Relevant conditions:
Cardiac Arrest
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the trial if you think are close to fitting criteria.
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Contact Information
Overall Contact
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Data sourced from ClinicalTrials.gov