Effect of Intraoperative Fluid Management on Morbidity

Not Applicable

Completed

• Conditions: Epidural Anesthesia

• Registration Number: NCT00156338
• Lead Sponsor: University Hospital Muenster

Brief Summary

The purpose of this study is to determine whether intraoperative fluid and sodium restriction decreases postoperative morbidity

Detailed Description

Not available

Study Timeline

• Study Start: 2005-07
• Study First Submitted: 2005-09-08
• Study First Submitted QC: 2005-09-08
• Study First Posted: 2005-09-12
• Primary Completion: 2009-12
• Study Completion: 2010-12
• Status Verified: 2012-01
• Last Update Submitted: 2012-01-16
• Last Update Posted: 2012-01-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 108

Inclusion Criteria

• epidural anesthesia
• ASA I-III

Exclusion Criteria

• metastasized cancer
• pregnancy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Primary Outcome Measures

Name	Time	Method
all cause Morbidity	one year

Secondary Outcome Measures

Name	Time	Method
Gastral and intestinal function	one year after surgery
all cause Mortality	one year

Trial Locations

Locations (3)

Raphaelsklinik; 🇩🇪 Münster, Germany

St. Franziskus-Hospital Münster; 🇩🇪 Münster, Germany

Department of Anesthesiology and Intensive Care, University Hospital Münster; 🇩🇪 Münster, Germany