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
60 participants
OBSERVATIONAL
2014-08-31
2014-09-30
Brief Summary
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Study design: simulated prospective monocentric randomized crossover trial. Participants and methods: Sixty professionals rescuers of the pre-hospital care unit of University Hospital of Caen (doctors, nurses and ambulance drivers) are enrolled to performed 10 minutes of continuous chest compression on manikin (ResusciAnne®, Laerdal), twice, with and without a feedback device (CPRmeter®). Correct compression score (the main criterion) is defined by reached target of rate, depth and leaning at the same time (recorded continuously).
Hypothesis: Feedback device delay fatigue effect arises during cardiopulmonary resuscitation.
Detailed Description
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Conditions
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Study Design
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CASE_CROSSOVER
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* refusal
18 Years
ALL
Yes
Sponsors
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University Hospital, Caen
OTHER
Responsible Party
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Principal Investigators
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Clement BULEON, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital of Caen
Locations
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University Hospital of Caen
Caen, , France
Countries
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Other Identifiers
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A14-D20-VOL.21
Identifier Type: -
Identifier Source: org_study_id