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Single-rescuer Pediatric Resuscitation

NCT02694900 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2016-03-15

No results posted yet for this study

Summary

The objective of this pilot study was to compare the manual chest compressions (CC) versus CC feedback device TrueCPR vs mechanical CC device LifeLine ARM during simulated pediatric cardiopulmonary resuscitation

Conditions

  • Chest Compression

Interventions

OTHER

Manually chest compressions

Chest compressions performed manually without any device

DEVICE

Cardiopump

Chest compressions performed with Cardiopump

DEVICE

LifeLine ARM

Chest compressions performed using mechanical chest compressions 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
2016-03-31
Completion
2016-03-31

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 NCT02694900 on ClinicalTrials.gov