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Perioperative Colloid vs Crystalloid in Patients Undergoing Colorectal Surgery

NCT01303250 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2015-12-18

No results posted yet for this study

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.

Conditions

  • Surgery, Colorectal

Interventions

DRUG

balanced 6% hydroxyethylstarch 130/0.4

Fluid administration and optimization based on cardiac output findings during surgery.

DRUG

balanced crystalloid

Fluid administration and optimization based on cardiac output findings during surgery.

Sponsors & Collaborators

  • Fresenius Kabi

    collaborator INDUSTRY

  • University Hospital Muenster

    lead OTHER

Principal Investigators

  • Hugo Van Aken, Prof. MD · Department of Anesthesia and Intensive Care, University Hospital Muenster

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2015-04-30
Completion
2015-04-30

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 NCT01303250 on ClinicalTrials.gov