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Human Electrical-Impedance-Tomography Reconstruction Models

Assessment of CT-derived Thoracic Electrical-Impedance-Tomography Finite Element Models

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02773680
Enrollment
160
Registered
2016-05-16
Start date
2016-05-31
Completion date
2017-06-30
Last updated
2016-05-16

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

Conditions

Respiratory Monitoring

Keywords

respiration, monitoring, physiologic, diagnostic techniques, respiratory system

Brief summary

Current EIT analyses are based on the assumption of a circular thorax-shape and do not provide any information on lung borders. The aim is to obtain the body and lung border contours of male subjects by multi-detector computed tomography (MDCT) in defined thresholds of anthropometric data (gender = male; height; weight) for calibration of more realistic EIT reconstruction models.

Detailed description

A major drawback of EIT is its relatively poor spatial resolution and its limitation in measuring changes in bioimpedance as compared to a reference state (and not absolute quantities). Therefore, the technique cannot differentiate between extrapulmonary structures (muscles, thorax, heart, large vessels, spine, etc.) and non-aerated lung tissues - which is a major limitation for the clinical use of information derived from EIT-imaging. Moreover, current EIT-reconstruction algorithms are based on the consideration of a complete circular thoracic shape and do not take into account the body contours and lung borders. The investigators are convinced that EIT-derived dynamic bedside lung imaging can be advanced by morphing computed tomography (CT) scans of the respective thoracic levels with concomitant EIT images - thus enhancing EIT-image information with CT-data. Integrating the anatomy of thoracic shape and lung borders provided by high-spatial resolution multi detector CT-scans (MDCT) with high-temporal resolution EIT has the potential to improve image quality considerably. This data can be used to compute mean EIT-reconstruction models that further offer the possibility to develop novel and clinically meaningful EIT parameters. Therefore, the investigators hypothesize that by integration of CT-scan information of body and lung contours (and by computing different EIT reconstruction models) the current methodological limitations of EIT technology can be overcome.

Interventions

DEVICEelectrical impedance tomography

One continous electrical impedance tomography (EIT) measurement per subject of approximately 5 minutes duration (2 min prior to MDCT scanning, during end-inspiratory MDCT acquisition and 2 min after MDCT scanning)

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* spontaneous breathing male subjects * age \> 18, * clinical indication for thoracic CT scanning, * matching of weight and height to the predefined model-thresholds

Exclusion criteria

* pre-existing chronic pulmonary disease * skin lesions / wounds in the thoracic plane where the EIT SensorBelt will be attached * known allergy against any ingredient of the used ContactAgent * abnormalities in thoracic shape as defined by the radiologist in charge (e.g. extreme kyphosis, funnel chest, pigeon breast, multiple rip fractures) * pneumothorax * pace maker (external and internal) * other implanted electrical devices * other methods measuring bioimpedance

Design outcomes

Primary

MeasureTime frameDescription
Electrical Impedance Tomography Finite Element Modelapproximately 1 year through study completionBased on CT-derived thorax, lung and heart contours we propose to calculate human finite element models (FEM) for EIT analysis

Secondary

MeasureTime frame
heightat the time-point of inclusion
weightat the time-point of inclusion
genderat the time-point of inclusion

Contacts

Primary ContactStefan Boehme, MD
stefan.boehme@meduniwien.ac.at+43 40400 41020

Outcome results

None listed

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