Clinical Trials Directory

Trials / Completed

CompletedNCT04215627

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

Comparison Between Invasive Hemodynamic Monitoring, Using the PiCCO Monitor, to a Non-invasive Photoplethysmography Based Device in Hemodynamic Unstable Critically Ill Patients, With Vasopressor Support

Status
Completed
Phase
Study type
Observational
Enrollment
9 (actual)
Sponsor
Biobeat Technologies Ltd. · Industry
Sex
All
Age
18 Years – 99 Years
Healthy volunteers

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.

Conditions

Interventions

TypeNameDescription
DEVICEnon-invasive monitoringComparing the PiCCO monitor to the non-invasive BB-613PW device in hemodynamically unstable critically ill patients in the ICU

Timeline

Start date
2019-12-26
Primary completion
2021-04-15
Completion
2021-04-30
First posted
2020-01-02
Last updated
2021-07-07

Locations

1 site across 1 country: Israel

Regulatory

Source: ClinicalTrials.gov record NCT04215627. Inclusion in this directory is not an endorsement.

Comparing the PiCCO Monitor to the Non-invasive Biobeat (BB)-316PW in ICU Patients (NCT04215627) · Clinical Trials Directory