Head and thorax elevation during cardiopulmonary resuscitation using circulatory adjuncts is associated with improved survival.
Johanna C Moore, Paul E Pepe, Kenneth A Scheppke...
https://pubmed.ncbi.nlm.nih.gov/35933057Actively Recruiting
Led by Hennepin Healthcare Research Institute · Updated on 2025-06-12
5000
Participants Needed
1
Research Sites
52 weeks
Total Duration
This research tracks the use and outcomes of a specialized approach to cardiac arrest care in emergency medical systems across the US and Europe. It focuses on patients who receive a combination of devices and techniques including a Head Up CPR positioning device, an impedance threshold device (ITD), and either manual active compression-decompression CPR or automated compression CPR. The registry aims to understand how this system of care is applied rapidly during cardiac arrest and its effects on patient outcomes. All patients in this observational registry receive the Head Up CPR based bundle of care, which includes multiple FDA-approved devices: manual or automated CPR methods combined with an ITD and an automated device that elevates the head and thorax in a controlled way. Emergency medical systems using these protocols submit de-identified data about their cardiac arrest cases, both before and after adopting the Head Up CPR bundle. Participants are monitored during cardiac arrest with continuous measurements such as end tidal CO2 and cerebral oximetry if available. Researchers collect data on return of spontaneous circulation, survival up to 60 days, and neurological function outcomes. The registry securely stores all patient data to study the effects of this device-assisted CPR method over time.
CONDITIONS
International Device Assisted Controlled Sequential Elevation CPR Registry
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to around 40 minutes during cardiac arrest
Participants undergo CPR using a Head Up CPR based bundle of care, which includes device assisted controlled elevation of the head and thorax along with CPR methods and an impedance threshold device.
1 emergency treatment episode
Duration - Up to 60 days
Participants are observed for survival and neurological function outcomes after the CPR intervention.
Total: 1 location
1
Hennepin Healthcare Research Institute
Minneapolis, Minnesota, United States, 55415
Actively Recruiting
J
Johanna C Moore, MD, MS
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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