Preconditioning Volatile Anesthesia in Liver Surgery

NCT01021228 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 257

Last updated 2009-11-26

No results posted yet for this study

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.

Conditions

  • Anesthesia

Sponsors & Collaborators

  • University of Zurich

    lead OTHER

Principal Investigators

  • Ksenija Slankamenac, med. pract · Departement of Visceral and Transplantation

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2009-10-31
Completion
2009-10-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01021228 on ClinicalTrials.gov