Study Results
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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COMPLETED
NA
52 participants
INTERVENTIONAL
2016-02-29
2016-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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Resuscitation on the flor
2 min asynchronous cardiopulmonary resuscitation. The patient lies on the floor
Manually chest compressions
Chest compressions performed manually without any device
Cardiopump
Chest compressions performed with Cardiopump
LifeLine ARM
Chest compressions performed using mechanical chest compressions system LifeLine ARM
Resuscitation on the stretcher
2 min asynchronous cardiopulmonary resuscitation. The patient lies on a stretcher
Manually chest compressions
Chest compressions performed manually without any device
Cardiopump
Chest compressions performed with Cardiopump
LifeLine ARM
Chest compressions performed using mechanical chest compressions system LifeLine ARM
Interventions
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Manually chest compressions
Chest compressions performed manually without any device
Cardiopump
Chest compressions performed with Cardiopump
LifeLine ARM
Chest compressions performed using mechanical chest compressions system LifeLine ARM
Eligibility Criteria
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Inclusion Criteria
* maximum 1 year of work experience in medicine
* minimum 10 clinical resuscitations
* paramedics, nurses, physicians
Exclusion Criteria
* wrist or low back diseases
* pregnancy
18 Years
65 Years
ALL
Yes
Sponsors
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Medical University of Warsaw
OTHER
Responsible Party
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Łukasz Szarpak
Principal Investigator
Locations
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Łukasz Szarpak
Warsaw, , Poland
Countries
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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.
Other Identifiers
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02.009.1MR
Identifier Type: -
Identifier Source: org_study_id
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