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The Haemodynamic Effects of Mechanical Standard and Active Chest Compression-decompression During Out-of-hospital CPR

NCT02479152 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2017-08-04

No results posted yet for this study

Summary

The aim of this randomized out-of-hospital cardiopulmonary resuscitation study is to investigate haemodynamics generated by the standard mechanical external chest compression device (LUCAS™ 2) compared to a new version generating chest compressions and active decompression above the initial starting position of the suction cup (LUCAS™ 2AD).

Conditions

  • Cardiac Arrest

Interventions

DEVICE

LUCAS2 AD

LUCAS™ 2AD with compressions like the standard LUCAS™ 2 but added decompressions above the initial start position.

Sponsors & Collaborators

  • GE Healthcare

    collaborator INDUSTRY

  • Physio-Control

    lead INDUSTRY

Principal Investigators

  • Lars Wik, MD, PhD · Oslo Universitetssykehus. Ullevål, Norway.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2017-04-30
Completion
2017-04-30

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02479152 on ClinicalTrials.gov