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Preconditioning Volatile Anesthesia in Liver Surgery

NCT ID: NCT01021228

Last Updated: 2009-11-26

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

257 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-08-31

Study Completion Date

2009-10-31

Brief Summary

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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

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

Conditions

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Anesthesia

Keywords

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Liver resection Continuous volatile anesthesia Continuous intravenous anesthesia Preconditioning volatile anesthesia Comparing three groups of anesthesia during the liver surgery according to their benefit on liver and outcome.

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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group1

continuous volatile anesthesia (sevoflurane) during the liver resection

No interventions assigned to this group

group2

continuous intravenous anesthesia (propofol) during the liver resection

No interventions assigned to this group

group3

preconditioning volatile anesthesia (sevoflurane) 30 minutes before ischemia (inflow occlusion)

No interventions assigned to this group

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Zurich

OTHER

Sponsor Role lead

Responsible Party

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Department of Visceral and Transplantation Surgery

Principal Investigators

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Ksenija Slankamenac, med. pract

Role: PRINCIPAL_INVESTIGATOR

Departement of Visceral and Transplantation

Locations

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Universtiy Hospital of Zurich, Department of Visceral and Transplantation Surgery

Zurich, Canton of Zurich, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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StV 18-2008

Identifier Type: -

Identifier Source: org_study_id