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
46 participants
INTERVENTIONAL
2014-04-30
2014-10-31
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
DIAGNOSTIC
NONE
Study Groups
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Control
The investigators measure quality of chest compressions before nightshift. Control group
CPR
Simulated cardiac arrest on a manikin Chest Compression CPR for 6 minutes
OFF
The investigators measure quality of chest compressions before nightshift. After night shift group
CPR
Simulated cardiac arrest on a manikin Chest Compression CPR for 6 minutes
Interventions
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CPR
Simulated cardiac arrest on a manikin Chest Compression CPR for 6 minutes
Eligibility Criteria
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Inclusion Criteria
* Resident / Physicians in Intensive Care Unit (ICU) or taking night in ED
* Nightshift \> 18 hours
Exclusion Criteria
ALL
Yes
Sponsors
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Bistro Study Group
OTHER
Responsible Party
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Yonathan Freund
Doctor
Principal Investigators
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Yonathan Freund
Role: PRINCIPAL_INVESTIGATOR
Emergency Department, Hôpital Pitié-Salpêtrière, 47-83 Boulevard de l'Hôpital, 75013 Paris, France.
Locations
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Hôpital Pitié-Salpêtrière; Hopital Saint Antoine; Hopital Tenon
Paris, , France
Countries
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Other Identifiers
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BG-CAN
Identifier Type: -
Identifier Source: org_study_id
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