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Combining Electrical Impedance Tomography and Thoracic Ultrasound Toinvestigate Dynamic Changes

Combining Electrical Impedance Tomography and Thoracic Ultrasound to Investigate Dynamic Changes of Respiratory Effort, and Regional & End-expiratory Lung Volume in Mechanically Ventilated Patients.

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06958770
Enrollment
50
Registered
2025-05-06
Start date
2025-05-19
Completion date
2028-12-31
Last updated
2025-05-06

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

Conditions

ARDS (Moderate or Severe)

Keywords

Chest ultrasound, electrical impedance tomography

Brief summary

1. To evaluate the dynamic changes of lung ultrasound during electrical impedance tomography (EIT) PEEP titration and across the first week of ARDS. 2. To asses respiratory effort by diaphragmatic function, esophageal pressure, and EIT (Pendelluft phenomenon), and hyperinflammatory biomarkers, to predict P-SILI. 3. To develop predictive models for weaning success based on integrated EELI and thoracic ultrasound.

Interventions

DIAGNOSTIC_TESTElectrical impedance tomography

* Electrical impedance tomography (EIT):Assessing pulmonary function in chronic lung diseases. * Lung ultrasound:Assessing diaphragm atrophy in mechanically ventilated patients. * Esophageal pressure:The work of breathing, or the energy required by respiratory muscles to meet ventilatory demands, can be directly evaluated by esophageal pressure * Oxygen consumption:Indirectly evaluated by measuring oxygen consumption (V̇O2) during mechanical ventilation The oxygen cost of breathing, reflected the increase in V̇O2 when transitioning from mechanical ventilation to spontaneous breathing, has been shown to predict weaning outcomes.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Adult \>18 y/o. * Patient intubated and receiving mechanical ventilation \> 24 hours. * Admitted into ICU, diagnosed as moderate or severe ARDS (ICD-10-CM: J80) according to Berlin definition.

Exclusion criteria

* Presence of Implanted Electronic Devices (pacemakers, implantable cardioverter-defibrillators). * Pregnancy. * No consent/inability to obtain consent and appropriate legal representative not available.

Design outcomes

Primary

MeasureTime frameDescription
ARDSFrom enrollment to the end of treatment at 1 weeks.Correlation of LUS aeration scores and overdistension metrics (e.g., A-line prominence, reduced lung sliding) with EIT parameters, including hyperdistension (%), collapse (%), and ΔEELI. Correlation of P-SILI risk with diaphragmatic function (ultrasound-measured excursion and thickening fraction), esophageal pressure variations (ΔPes, ΔPdi), pendelluft dynamics (phase shift, amplitude difference from EIT), and hyperinflammatory biomarkers (e.g., IL-6, IL-8).

Contacts

Primary ContactYao-Wen Kuo
kyw@ntu.edu.tw886+972651821

Outcome results

None listed

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