Actively Recruiting

Age: 18Years +
All Genders
NCT06544148

Non-Invasive Measurements of Changes in Pulmonary Artery Pressure in Intensive Care Unit Patients Using Electrical Impedance Tomography - A Feasibility Study

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2024-11-14

28

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

I

Insel Gruppe AG, University Hospital Bern

Lead Sponsor

C

CSEM Centre Suisse d'Electronique et de Microtechnique SA - Recherche et Developpement

Collaborating Sponsor

AI-Summary

What this Trial Is About

To assess whether changes in electrical impedance - measured using an electrical impedance tomography (EIT) chest belt - can be used to derive changes in pulmonary artery pressure (PAP) in critically ill patients when compared to invasive gold-standard PAP measured using pulmonary artery catheter (PAC).

CONDITIONS

Official Title

Non-Invasive Measurements of Changes in Pulmonary Artery Pressure in Intensive Care Unit Patients Using Electrical Impedance Tomography - A Feasibility Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Intubated patients in the ICU with clinical decision to monitor pulmonary artery pressure and cardiac output using a pulmonary artery catheter
Not Eligible

You will not qualify if you...

  • Patients with implanted or external thoracic electronic devices or thoracic metal implants
  • Known pregnancy or lactating patients
  • Open lung injuries or pneumothorax
  • Open wounds, drainages, burns, or rashes on the upper chest
  • Thoracic perimeter smaller than 66 cm or larger than 134 cm
  • Known allergies to wound dressings or adhesives such as gel electrodes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Inselspital Bern, Universitätsklinik für Intensivmedizin

Bern, Switzerland, 3010

Actively Recruiting

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Research Team

K

Kaspar F Bachmann, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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