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Non-invasive Measurement of Central Hemodynamics by Electrical Impedance Tomography

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

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01412970
Enrollment
0
Registered
2011-08-09
Start date
2016-07-31
Completion date
2017-03-31
Last updated
2022-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Comparison of Availability for Prediction of Volume Responsiveness, Comparison of Limits of Agreement for Invasive and Non-invasive Measurement of Stroke Volume Variation

Keywords

hemodynamic monitoring, volume responsiveness, electrical impedance tomography

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.

Interventions

volume loading according to functional parameters of cardiac preload, i.e. stroke volume variations measured by arterial pulse contour analysis

Sponsors

CSEM Centre Suisse d'Electronique et de Microtechnique SA - Recherche et Developpement
CollaboratorINDUSTRY
Oregon Health and Science University
CollaboratorOTHER
Universitätsklinikum Hamburg-Eppendorf
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Ability to assess volume responsiveness by electrical impedance tomographywithin 3 hrs after surgical procedureAssessment of volume responsiveness by electrical impedance tomography in mechanically ventilated patients by measurement of stroke volume variations under stepwise volume loading

Secondary

MeasureTime frameDescription
precision of estimation of non invasive measurement of stroke volume variationwithin 3 hours after surgeryprecision of estimation of non invasive measurement of stroke volume variation by electrical impedance tomography in comparison to clinically established, invasive advanced hemodynamic monitoring devices

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026