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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInsel Gruppe AG, University Hospital Bern

About this trial

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).

Eligibility criteria

Qualifiers

Age ≥ 18-year-old.

Intubated patients in the ICU with clinical decision to monitor PAP and cardiac output using a PAC.

Disqualifiers

Patients with implanted or external thoracic electronic devices (e.g., pacemaker) or thoracic metal implants.

Known pregnancy or lactating patients.

Open lung injuries or pneumothorax.

Open wounds, drainages, burns or rashes of the upper thorax.

Trial design

Treatments tested in this trial

  • Electrical impedance tomography

Treatment groups

28 Participants
are divided into 1 treatment group

Sponsors and collaborators

Insel Gruppe AG, University Hospital Bern

Lead sponsor

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

Collaborator