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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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3 August 2015 |
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Main ID: |
NCT02123810 |
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Date of registration:
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22/04/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Quality of Chest Compressions After a Night Shift
WeCAN |
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Scientific title:
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Weaker Chest Compression After Nightshift : The We CAN Study. |
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Date of first enrolment:
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April 2014 |
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Target sample size:
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46 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02123810 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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Phase:
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N/A
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Countries of recruitment
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France
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Contacts
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Name:
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Yonathan Freund |
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Address:
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Telephone:
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Email:
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Affiliation:
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Emergency Department, Hôpital Pitié-Salpêtrière, 47-83 Boulevard de l'Hôpital, 75013 Paris, France. |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Resident / Physicians in emergency departement (ED) or taking night in ED
- Resident / Physicians in Intensive Care Unit (ICU) or taking night in ED
- Nightshift > 18 hours
Exclusion Criteria:
- Stop chest compressions before 2 minutes
Age minimum:
N/A
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Cardiac Arrest
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Intervention(s)
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Other: CPR
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Primary Outcome(s)
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the proportion of CC with a depth higher than 50mm
[Time Frame: 2 minutes of chest compressions]
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Secondary Outcome(s)
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Number of chest compressions
[Time Frame: 2 minutes]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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