International Device Assisted Controlled Sequential Elevation CPR Registry

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
United States
Minnesota
Hennepin Healthcare Research Institute
RECRUITING
Minneapolis
Contact Information
Primary
Johanna C Moore, MD, MS
johanna.moore@hcmed.org
612 873 4908
Time Frame
Start Date: 2020-03-23
Estimated Completion Date: 2027-06
Participants
Target number of participants: 5000
Treatments
Head Up CPR based bundle of care
All patients in the registry receive the Head Up CPR based bundle of care.
Related Therapeutic Areas
Sponsors
Leads: Hennepin Healthcare Research Institute

This content was sourced from clinicaltrials.gov