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Clinical Trials/NCT01021228
NCT01021228
Completed
N/A

Preconditioning is Indeed Protective

University of Zurich1 site in 1 country257 target enrollmentAugust 2008
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ConditionsAnesthesia

Overview

Phase
N/A
Intervention
Not specified
Conditions
Anesthesia
Sponsor
University of Zurich
Enrollment
257
Locations
1
Primary Endpoint
peak ALT and AST levels representing the ischemia-reperfusion injury
Status
Completed
Last Updated
16 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to compare the impact and outcome of continuous volatile anesthesia to continuous intravenous anesthesia and to preconditioning volatile anesthesia in liver surgery.

Detailed Description

Comparing the impact and outcome of continuous volatile anesthesia to continuous intravenous anesthesia and to preconditioning volatile anesthesia in liver surgery.

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
October 2009
Last Updated
16 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •\> 18 years
  • •benign and malign disease
  • •any type of liver surgery
  • •inflow occlusion during the liver surgery

Exclusion Criteria

  • •\< 18 years
  • •participation on other interventional and treatment randomized controlled trials,
  • •trauma of the liver
  • •liver cirrhosis

Outcomes

Primary Outcomes

peak ALT and AST levels representing the ischemia-reperfusion injury

Time Frame: post-operative

Secondary Outcomes

  • length of hospital stay, length of ICU stay, blood loss and morbidity (post-operative complications)(post-operative)

Study Sites (1)

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