International Device Assisted Controlled Sequential Elevation CPR Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorHennepin Healthcare Research Institute

About this trial

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.

Eligibility criteria

Qualifiers

Patient is at least 18 years of age

Patient is in active cardiac arrest, as defined by presence of either ventricular fibrillation or ventricular tachycardia, or pulseless electrical activity, or asystole at time of enrollment.

Patient receives either a) active-compression decompression cardiopulmonary resuscitation b) automated suction-cup based CPR with an impedance threshold device (ITD) c) manual CPR with an ITD

Subject receives device assisted controlled elevation of the head and thorax.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Head Up CPR based bundle of care

Treatment groups

5,000 Participants
are divided into 1 treatment group