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Effect of Intraoperative Fluid Management on Morbidity

NCT00156338 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 108

Last updated 2012-01-18

No results posted yet for this study

Summary

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

Conditions

  • Epidural Anesthesia

Interventions

PROCEDURE

fluid management

volume and sodium restriction

PROCEDURE

fluid management

volume restriction

PROCEDURE

fluid management

liberal fluid management

Sponsors & Collaborators

  • University Hospital Muenster

    lead OTHER

Principal Investigators

  • Martin Westphal, MD · Department of Anesthesiology and Intensive Care, University Hospital Münster

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
FACTORIAL

Eligibility

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

Timeline & Regulatory

Start
2005-07-31
Primary Completion
2009-12-31
Completion
2010-12-31

Countries

  • Germany

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 NCT00156338 on ClinicalTrials.gov