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
260 participants
OBSERVATIONAL
2008-07-31
2017-04-21
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Study group
Patients undergoing major abdominal surgery
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Male or female
* Informed consent
* Major abdominal surgery
Exclusion Criteria
* Pre-existing severe renal or liver failure
* Chemo- or radiochemotherapy
18 Years
85 Years
ALL
No
Sponsors
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Klinikum St. Georg gGmbH
OTHER
Responsible Party
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Armin Sablotzki, MD
Prof. Dr. med.
Principal Investigators
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Armin R Sablotzki, MD
Role: PRINCIPAL_INVESTIGATOR
Klinikum St. Georg gGmbH
Locations
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Klinikum St. Georg gGmbH
Leipzig, Saxony, Germany
Countries
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Related Links
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Related Info
Other Identifiers
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Stu08/0022
Identifier Type: -
Identifier Source: secondary_id
EK-BR-21/08-1
Identifier Type: -
Identifier Source: org_study_id
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