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Comparing the PiCCO Monitor to the Non-invasive Biobeat (BB)-316PW in ICU Patients

Comparing the PiCCO Monitor to the Non-invasive Biobeat (BB)-316PW in ICU Patients

Recruiting
18-99 years
All
Phase N/A

Overview

The aim of this study is to compare hemodynamic monitoring using the invasive PiCCO device to the BB-613PW wireless, non-invasive PPG-based device, in critically ill patients within the ICU, suffering from hemodynamic instability and in need of vasopressor support. Data will be gathered prospectively and analysed retrospectively.

Eligibility

Inclusion Criteria:

  • ICU adult patients in the need of vasopressor support of more than 0.2 mcg/Kg/Min for a period longer than 3 hours
  • Patients in which PiCCO monitoring is needed

Exclusion Criteria:

  • Refusal of the subject
  • Technical difficulties in insertion of the PiCCO catheters
  • Significant cardiac arrhythmias
  • Significant valvular disease
  • Pregnancy

Study details
    Critical Illness
    Hemodynamic Instability

NCT04215627

Biobeat Technologies Ltd.

16 February 2024

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