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
PHASE4
200 participants
INTERVENTIONAL
2008-02-29
2009-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Observation
Observation
Data Collection
Collection of patient data before implementation of a nutritional management protocol
Nutritional management protocol
Collection of patient data after implementation of a nutritional management protocol
Nutritional management protocol
Collection of patient data after implementation of a nutritional management protocol
Interventions
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Data Collection
Collection of patient data before implementation of a nutritional management protocol
Nutritional management protocol
Collection of patient data after implementation of a nutritional management protocol
Eligibility Criteria
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Exclusion Criteria
* stay less than 72 hours on ICU
* die within 72h after admission
* patients admitted for palliative care
18 Years
ALL
No
Sponsors
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Abbott Nutrition
INDUSTRY
Insel Gruppe AG, University Hospital Bern
OTHER
Responsible Party
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Department of Intensive Care Medicine, Bern University Hospital, and University of Bern, Switzerland
Principal Investigators
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Michele Leuenberger, MD
Role: PRINCIPAL_INVESTIGATOR
University hospital of Bern
Stephan M Jakob, MD, PHD
Role: STUDY_DIRECTOR
University hospital of Bern
Zeno Stanga, MD
Role: PRINCIPAL_INVESTIGATOR
University hospital of Bern
Margaret Schafer, MD
Role: PRINCIPAL_INVESTIGATOR
University hospital of Bern
Jukka Takala, MD, PHD
Role: STUDY_CHAIR
University hospital of Bern
Other Identifiers
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ICU Nutr Bern
Identifier Type: -
Identifier Source: org_study_id
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