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Clinical Trials/NCT01412970
NCT01412970
Withdrawn
N/A

Non-invasive Measurement of Central Hemodynamics and Heart-lung Interactions by Electrical Impedance Tomography

Universitätsklinikum Hamburg-Eppendorf1 site in 1 countryJuly 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Comparison of Availability for Prediction of Volume Responsiveness
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Locations
1
Primary Endpoint
Ability to assess volume responsiveness by electrical impedance tomography
Status
Withdrawn
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the ability to measure central hemodynamics and heart-lung interactions non-invasively by electrical impedance tomography and compare it to clinically established hemodynamic monitoring.

Detailed Description

The purpose of this study is to evaluate the ability to measure central hemodynamics and heart-lung interactions non-invasively by electrical impedance tomography and compare it to clinically established hemodynamic monitoring.

Registry
clinicaltrials.gov
Start Date
July 2016
End Date
March 2017
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age \>18 years
  • Indication for advanced invasive hemodynamic monitoring due to operative procedure
  • Necessity of postoperative invasive ventilation

Exclusion Criteria

  • Age \<18 years
  • known affections cardiac function
  • presence of cardiac arrhythmias
  • contraindication for placement of central venous or femoral artery catheter

Outcomes

Primary Outcomes

Ability to assess volume responsiveness by electrical impedance tomography

Time Frame: within 3 hrs after surgical procedure

Assessment of volume responsiveness by electrical impedance tomography in mechanically ventilated patients by measurement of stroke volume variations under stepwise volume loading

Secondary Outcomes

  • precision of estimation of non invasive measurement of stroke volume variation(within 3 hours after surgery)

Study Sites (1)

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