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Clinical Trials/DRKS00008769
DRKS00008769
Completed
Not Applicable

Evaluation of esCCO monitoring for continuous, non-invasive measurement of cardiac output - COKA

niversitätsklinikum GießenAbteilung für Anästhesiologie, Operative Intensivmedizin und Schmerztherapie0 sites35 target enrollmentFebruary 15, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Q05.9
Sponsor
niversitätsklinikum GießenAbteilung für Anästhesiologie, Operative Intensivmedizin und Schmerztherapie
Enrollment
35
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study evaluated the validity of the non-invasive esCCO monitoring for the assessment of CO and SV as well as their indices in pregnant patients undergoing minimally-invasive foetoscopic surgery for spina bifida. As such, a healthy and homogenous cohort of pregnant patients who underwent minimally-invasive foetoscopic surgery for spina bifida of their unborn child was investigated. Our study found that esCCO-derived parameters did not correlate with the results of the pulse contour analysis. Only COesCCO showed a weak correlation with COTPTD. Analogous results were found in a subanalysis investigating the influence of PACI on the performance of esCCO. Overall, esCCO underestimated CO, CI, SV, and SVI consistently. Supposing a tolerance of 10% deviation to the established TPTD, esCCO failed to achieve reliable results.

Registry
who.int
Start Date
February 15, 2019
End Date
November 30, 2018
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
niversitätsklinikum GießenAbteilung für Anästhesiologie, Operative Intensivmedizin und Schmerztherapie

Eligibility Criteria

Inclusion Criteria

  • gynecological patients; pregnant women with the indication for a fetoscopic procedure

Exclusion Criteria

  • Age \<18 years, atrial fibrillation, pacemaker

Outcomes

Primary Outcomes

Not specified

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