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Clinical Trial Summary

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


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00156338
Study type Interventional
Source University Hospital Muenster
Contact
Status Completed
Phase N/A
Start date July 2005
Completion date December 2010

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