Actively Recruiting
International Device Assisted Controlled Sequential Elevation CPR Registry
Led by Hennepin Healthcare Research Institute · Updated on 2025-06-12
5000
Participants Needed
1
Research Sites
375 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this prospective observational cardiopulmonary resuscitation (CPR) registry is to track the use and clinical outcomes from emergency medical systems across the US and Europe that have implemented a system of care approach applied rapidly to cardiac arrest that includes using the combination of an impedance threshold device (ITD), and either manual active compression-decompression (ACD) CPR device or automated compression device, with a Head Up CPR device.
CONDITIONS
Official Title
International Device Assisted Controlled Sequential Elevation CPR Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient is at least 18 years of age
- Patient is in active cardiac arrest, defined by ventricular fibrillation, ventricular tachycardia, pulseless electrical activity, or asystole at enrollment
- Patient receives either active-compression decompression CPR, automated suction-cup based CPR with an impedance threshold device, or manual CPR with an impedance threshold device
- Patient receives device assisted controlled elevation of the head and thorax during CPR
You will not qualify if you...
- Prisoners
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hennepin Healthcare Research Institute
Minneapolis, Minnesota, United States, 55415
Actively Recruiting
Research Team
J
Johanna C Moore, MD, MS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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