What this study is
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.
What's being tested
- Head Up CPR based bundle of care
Intervention · DEVICE
All patients in this registry receive the intervention, a Head Up Cardiopulmonary Resuscitation (CPR) based bundle of care. This bundle of care includes the use of multiple FDA approved devices. The components of the Head Up CPR bundle are 1) a single or combination of CPR methods including manual, active-compression decompression CPR, or automated suction-cup based CPR 2) An impedance threshold device 3) An automated patient positioning device capable of elevating the head and thorax
Study details
- Sponsor
- Hennepin Healthcare Research Institute
- Conditions
- Cardiac Arrest, Out-Of-Hospital
- Enrolling
- 5,000 people
- Starts
- 2020-03-23
- Est. completion
- 2027-06
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- 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.
You can't join if
- Prisoners
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openHennepin Healthcare Research Institute
Minneapolis, Minnesota, United States
Recruiting
Study team
Sponsor
Hennepin Healthcare Research Institute
Study ID 1281037
Principal investigator
Johanna C Moore, MD, MS
Hennepin Healthcare Research Institute
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.