International Device Assisted Controlled Sequential Elevation CPR Registry

Conditions

• Cardiac Arrest, Out-Of-Hospital

Eligibility Criteria

Sex

ALL

Age

18 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• Head Up CPR based bundle of care — 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

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.

Key Dates

Start date

Mar 23, 2020

Status verified

Jun 2025

Primary completion

Jun 30, 2026

Completion

Jun 30, 2027

Study Design

Enrollment

5,000 participants (estimated)

Arms

• Arm: Head Up CPR based bundle of care
  All patients in the registry receive the Head Up CPR based bundle of care.

Primary Outcome Measure

Return of Spontaneous Circulation [ Time Frame: From the start of CPR to the presence of cardiac activity. The time period in which this outcome will varies and is estimated to range from 0 minutes up to around 40 minutes. ]

Central Contacts

• Johanna C Moore, MD, MS
  612 873 4908
  [email protected]

Locations (1)

Find similar trials in Minneapolis, MN

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