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
NA
125 participants
INTERVENTIONAL
2008-01-31
2010-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Sevoflurane
Sevoflurane for pharmacological postconditioning
Sevoflurane
3.2 Vol % for postconditioning
Propofol
Anesthesia maintenance with propofol instead of Sevoflurane postconditioning
Sevoflurane
3.2 Vol % for postconditioning
Interventions
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Sevoflurane
3.2 Vol % for postconditioning
Eligibility Criteria
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Inclusion Criteria
* patients undergoing liver resection (benign or malignant tumors)
Exclusion Criteria
* laparoscopic liver resection
* coagulopathy (platelets \< 50'000/ml, Quick \< 50%)
* liver cirrhosis
18 Years
90 Years
ALL
No
Sponsors
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University of Zurich
OTHER
Responsible Party
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University Hospital Zurich, Department of Anesthesiology
Principal Investigators
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01 Studienregister MasterAdmins
Role: STUDY_DIRECTOR
UniversitaetsSpital Zuerich
Locations
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University Hospital of Zurich
Zurich, , Switzerland
Countries
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Other Identifiers
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StV 34-2007
Identifier Type: -
Identifier Source: org_study_id
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