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Clinical Trials/NCT00468793
NCT00468793
Completed
Phase 4

Randomized Clinical Study of Traditional Versus ScvO2 Guided Perioperative Fluid Therapy

Haukeland University Hospital1 site in 1 country240 target enrollmentApril 2007
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ConditionsPerioperative Care

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Perioperative Care
Sponsor
Haukeland University Hospital
Enrollment
240
Locations
1
Primary Endpoint
Postoperative morbidity
Status
Completed
Last Updated
16 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Perioperative goal directed fluid therapy by means of an esophageal doppler has been shown to reduce morbidity and length of stay. In this study patients undergoing elective bowel surgery will be randomised to traditional fluid therapy with crystalloids versus fluid boluses guided by central venous oxygen saturation. The primary outcome will be complications after surgery.

Registry
clinicaltrials.gov
Start Date
April 2007
End Date
May 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Haukeland University Hospital

Eligibility Criteria

Inclusion Criteria

  • •Elective bowel surgery,
  • •Able to give informed consent

Exclusion Criteria

  • •Coagulation defect,
  • •Renal failure,
  • •Valvular stenosis

Outcomes

Primary Outcomes

Postoperative morbidity

Time Frame: postoperative day 30

Secondary Outcomes

  • serum creatinine(postoperative day 3)

Study Sites (1)

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