Non-invasive monitoring: Comparing blood pressure measurement using the Biobeat non-invasive monitor to arterial line.
Study summary
In this clinical study the investigators will compare blood pressure measurements obtained using the non-invasive, wireless Biobeat monitoring device (both a wrist watch and a patch configuration) to an invasive arterial line catheter (radial or femoral) and a Swan Ganz Catheter in 20 patients immediately after cardiac surgery, at the cardiac intensive care unit.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* 18 years old and above patients of both sexes arriving immediately after cardiac surgery to the intensive care unit with a radial/femoral arterial line and or a Swan Ganz catheter and in need for blood pressure monitoring.
Exclusion Criteria:
* Refusal to participate
* Patients with no need or no technical capability to have an arterial line
* Pregnant women
* Individuals under the age of 18 years
* Patients with lack of judgment/mental illness
* Patients working in the Sheba Medical Center
Primary outcome measure(s)
Level of accordance between the Biobeat monitor and the arterial line — 4 hours per individual Comparing blood pressure measurements of the Biobeat device with those of the arterial line. Both systolic blood pressure and diastolic blood pressure will be assessed during the study period.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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