Chest Compression During Resuscitation

NCT ID: NCT02703103

Last Updated: 2016-04-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-02-29

Study Completion Date

2016-04-30

Brief Summary

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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.

Detailed Description

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Conditions

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Cardiopulmonary Resuscitation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Standard cardiopulmonary resuscitation

standard CPR (30:2) according to European Resuscitation Council 2015 guidelines for cardiopulmonary resuscitation.

Group Type EXPERIMENTAL

Manual chest compressions

Intervention Type OTHER

2 min of Chest compressions without mechanical chest compression system

ARM chest compressions

Intervention Type DEVICE

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

asynchronous cardiopulmonary resuscitation

asynchronuos CPR according to European Resuscitation Council 2015 guidelines for cardiopulmonary resuscitation.

Group Type EXPERIMENTAL

Manual chest compressions

Intervention Type OTHER

2 min of Chest compressions without mechanical chest compression system

ARM chest compressions

Intervention Type DEVICE

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

Interventions

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Manual chest compressions

2 min of Chest compressions without mechanical chest compression system

Intervention Type OTHER

ARM chest compressions

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

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* give voluntary consent to participate in the study
* maximum 1 year of work experience in medicine
* minimum 10 clinical resuscitations
* paramedics

Exclusion Criteria

* not meet the above criteria
* wrist or low back diseases
* pregnancy
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Medical University of Warsaw

OTHER

Sponsor Role lead

Responsible Party

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Łukasz Szarpak

Łukasz Szarpak

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Łukasz Szarpak

Warsaw, , Poland

Site Status RECRUITING

Countries

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Poland

Central Contacts

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Lukasz Szarpak, PhD

Role: CONTACT

500186225

Facility Contacts

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Łukasz Szarpak

Role: primary

500186225

References

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Truszewski Z, Szarpak L, Kurowski A, Evrin T, Zasko P, Bogdanski L, Czyzewski L. Randomized trial of the chest compressions effectiveness comparing 3 feedback CPR devices and standard basic life support by nurses. Am J Emerg Med. 2016 Mar;34(3):381-5. doi: 10.1016/j.ajem.2015.11.003. Epub 2015 Nov 4.

Reference Type BACKGROUND
PMID: 26612703 (View on PubMed)

Kurowski A, Czyzewski L, Bogdanski L, Zasko P, Karczewska K, Szarpak L. Quality of chest compression with CardioPump CPR compared to single rescuer standard BLS. Am J Emerg Med. 2015 Jan;33(1):114-5. doi: 10.1016/j.ajem.2014.10.027. Epub 2014 Oct 20. No abstract available.

Reference Type BACKGROUND
PMID: 25455057 (View on PubMed)

Other Identifiers

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02.008.1MR

Identifier Type: -

Identifier Source: org_study_id

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