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

I

Insel Gruppe AG, University Hospital Bern

Status

Enrolling

Conditions

Pulmonary Artery Hypertension

Treatments

Device: Electrical impedance tomography

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT06544148
2024-00435

Details and patient eligibility

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).

Enrollment

28 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18-year-old.
  • Intubated patients in the ICU with clinical decision to monitor PAP and cardiac output using a PAC.

Exclusion criteria

  • 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.
  • Estimated thoracic perimeter smaller than 66 cm or larger than 134 cm.
  • Known allergies to wound dressings or adhesives (e.g., gel electrodes)

Trial design

28 participants in 1 patient group

All Study Participants
Treatment:
Device: Electrical impedance tomography

Trial contacts and locations

1

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Central trial contact

Kaspar F Bachmann, MD

Data sourced from clinicaltrials.gov

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