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OpenTrials
Completed

NCT Number: NCT00156338

Effect of Intraoperative Fluid Management on Morbidity

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

Completed

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Key information

Conditions

Epidural Anesthesia

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Anesthesiology and Intensive Care, University Hospital Münster, Münster, Germany

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • epidural anesthesia
  • ASA I-III

Exclusion criteria

  • metastasized cancer
  • pregnancy

Treatment and study plan

fluid management

Procedure

volume and sodium restriction

Primary outcomes

  1. all cause Morbidity

    Time frame: one year

Secondary outcomes

  1. Gastral and intestinal function

    Time frame: within the first 30 days after surgery

  2. all cause Mortality

    Time frame: one year

  3. Gastral and intestinal function

    Time frame: one year after surgery

Sponsors and collaborators

Lead sponsor

University Hospital Muenster

Other

Registry information

Official study title

Effect of Intraoperative Fluid Management on Morbidity in Patients Undergoing Colorectal Surgery

Important dates

Study start
2005
Primary completion
2009
Study completion
2010
First posted
Sep 12, 2005
Registry last updated
Jan 18, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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