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
215 participants
OBSERVATIONAL
2012-04-30
2013-08-31
Brief Summary
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Detailed Description
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After written information and consent, an independent, specially trained investigator interviews residents, doctors and nurses in charge of the patient and ask them how they rates patients capacity.
Conditions
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Study Design
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CROSS_SECTIONAL
Study Groups
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Decision making
Patient's capacity
Interventions
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Patient's capacity
Eligibility Criteria
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Inclusion Criteria
Doctors, hospital interns, nurses state of both sexes, aged 18 years or more working in Intensive Care, members of a social security system engaged in a clinic on the day of the assessment
* Patients :
Patients of both sexes, aged 18 years or more hospitalized in Intensive Care, members of a social security system
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital, Clermont-Ferrand
OTHER
Responsible Party
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Principal Investigators
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Alexandre LAUTRETTE
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Clermont-Ferrand
Locations
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CHU Clermont-Ferrand
Clermont-Ferrand, , France
Countries
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Other Identifiers
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2011-A01492-39
Identifier Type: -
Identifier Source: secondary_id
CHU-0164
Identifier Type: -
Identifier Source: org_study_id
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