Clinical Trials Directory

Trials / Completed

CompletedNCT00380107

Volume Deficit Prior to Surgery

Estimation of Volume Deficit in Patients Prior to Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
4 (actual)
Sponsor
Rigshospitalet, Denmark · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Accepted

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.

Conditions

Timeline

Start date
2006-10-01
Primary completion
2007-08-01
Completion
2007-08-01
First posted
2006-09-25
Last updated
2009-08-06

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00380107. Inclusion in this directory is not an endorsement.