Perioperative Colloid vs Crystalloid in Patients Undergoing Colorectal Surgery — KoKris  

Surgery, Colorectal Clinical Trial

Official title: Balanced 6 % HES 130/0.4 vs. Balanced Crystalloid-based Infusion in Patients Undergoing Colorectal Surgery

Status Terminated

Clinical Trial Summary

The primary purpose of this study is to determine the effect of a balanced 6%hydroxyethyl starch 130/0.4 vs. a balanced crystalloid in colorectal surgery. The intraoperative fluid management will be given to optimize the stroke volume variation <= 12%.

The investigators hypothesize that patients in the intervention group will need less fluid administration be optimal hemodynamic stabilized.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Surgery, Colorectal

• NCT number: NCT01303250
• Study type: Interventional
• Source: University Hospital Muenster
• Status: Terminated
• Phase: Phase 4
• Start date: April 2011
• Completion date: April 2015