Clinical Trials Directory

Trials / Completed

CompletedNCT02277353

Evaluation of SVV From NICOM as a Predictor of Fluid Responsiveness in Prone Position During Spine Surgery

Evaluation of Stroke Volume Variation Derived From NICOM as a Predictor of Fluid Responsiveness in Prone Position During Spine Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
40 (actual)
Sponsor
Samsung Medical Center · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

NICOM® is a recently developed noninvasive cardiac output monitoring device, and indices derived from NICOM® such as SVV has been reported to predict fluid responsiveness in the previous studies. However, its usefulness in prone positioning has not been investigated. Thus, the aim of this prospective observational study is to evaluate the usefulness of stroke volume variation (SVV) derived from NICOM® to predict fluid responsiveness in prone patients undergoing spine surgery.

Conditions

Interventions

TypeNameDescription
OTHERFluid loading to evaluate fluid responsivenessloading of hydroxyethyl starch 6ml/kg over 10-15min to all patients

Timeline

Start date
2014-10-01
Primary completion
2015-06-01
Completion
2015-06-01
First posted
2014-10-29
Last updated
2015-07-21

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02277353. Inclusion in this directory is not an endorsement.