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Clinical Trials/NCT00380107
NCT00380107
Completed
Not Applicable

Estimation of Volume Deficit in Patients Prior to Surgery

Rigshospitalet, Denmark1 site in 1 country4 target enrollmentOctober 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypovolemia
Sponsor
Rigshospitalet, Denmark
Enrollment
4
Locations
1
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

It is the purpose of the researchers to identify the variation in intravascular deficits which can have relevance in high risk patients for minor and medium sized surgery.

The investigators will also estimate fluid deficit in healthy, non-fasting subjects for comparison.

Detailed Description

Intravascular volume optimization has shown to improve outcome after surgery. In minor and medium surgery , however, the preoperative volume deficit has not been estimated with functional parameters. Patient scheduled for minor surgery are included. After the patient is anesthetized the intravascular volume is optimized by stroke volume maximization by colloid boluses. Stroke volume is obtained by esophageal Doppler technique which is a minimally invasive method. The volume estimated for optimization is considered as the functional volume deficit. In the healthy subjects the probe will be placed in the awake subject. A standardized meal and fluid intake secures that the subjects are in a non-fasting state.

Registry
clinicaltrials.gov
Start Date
October 2006
End Date
August 2007
Last Updated
16 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Planned minor or medium sized surgery

Exclusion Criteria

  • Oesophageal pathology
  • Age \>90 yr or \< 18 yr
  • Alcohol abuse,
  • Insulin dependent DM

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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