Impaired Preoperative Nutritional Status as a Risk Factor for Postoperative Clinical Outcome
NCT ID: NCT01492946
Last Updated: 2017-01-23
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
400 participants
OBSERVATIONAL
2010-05-31
2012-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Elective surgical patients
Elective surgical patients in the Charité University Berlin Campus Charité Mitte
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Patients must be 18 years or older
3. Ambulation
4. ASA-Score I-IV
5. bioelectrical impedance analysis to determine the phase angle
Exclusion Criteria
2. Pregnancy
3. ASA Score V-VI
4. Amputated limbs
5. Pacemaker and defibrillators
6. Cerebrovascular events
7. Tattoos on the electrode locations
18 Years
ALL
No
Sponsors
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Charite University, Berlin, Germany
OTHER
Responsible Party
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Claudia Spies
study director
Principal Investigators
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Claudia Spies, MD Prof.
Role: STUDY_DIRECTOR
Department of Anesthesiology and Operative Intensive Care Medicine Campus Charité Mitte, Charite University, Berlin, Germany
Locations
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Department of Anesthesiology and Operative Intensive Care Medicine Campus Charité Mitte, Charite University,
Berlin, State of Berlin, Germany
Countries
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Other Identifiers
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PreopBIA
Identifier Type: -
Identifier Source: org_study_id
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