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Chest Compression During Resuscitation

NCT02703103 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2016-04-06

No results posted yet for this study

Summary

The aim of the study was to evaluate the new mechanical chest compression machine LifeLine ARM in healthcare professionals in simulated model of cardiac arrest.

Conditions

  • Cardiopulmonary Resuscitation

Interventions

OTHER

Manual chest compressions

2 min of Chest compressions without mechanical chest compression system

DEVICE

ARM chest compressions

2 min of Chest compressions with mechanical chest compression system LifeLine ARM

Sponsors & Collaborators

  • Medical University of Warsaw

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-02-29
Primary Completion
2016-04-30
Completion
2016-04-30

Countries

  • Poland

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 NCT02703103 on ClinicalTrials.gov