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

  • STATUS
    Recruiting
  • participants needed
    30
  • sponsor
    Biobeat Technologies Ltd.
Updated on 19 February 2024
vasopressor
critically ill
hemodynamic instability

Summary

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.

Details
Condition Critical Illness, Hemodynamic Instability
Age 18-99 years
Treatment non-invasive monitoring
Clinical Study IdentifierNCT04215627
SponsorBiobeat Technologies Ltd.
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

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
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