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COMPLETEDNCT04215627

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

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...

Lead sponsor: Biobeat Technologies Ltd.•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Biobeat Technologies Ltd.

Collaborators

Assaf-Harofeh Medical Center

Age

18 - 99 years

Sex

ALL

Healthy Volunteers

No

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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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: July 7, 2021Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment9

Start dateDec 2019

Last updatedJul 7, 2021

Condition

Critically Ill Hemodynamic Instability

Locations shown

The Assaf Harofeh Medical Center, Zrifin

Rishon LeZiyyon

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: July 7, 2021Data synced to Clareo: July 13, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions