Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Blood Pressure
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Non-anaesthetized subjects in the ICU (Intensive Care Unit) or in the CICU (Cardiac Intensive Care Unit) with arterial line placement in the radial artery.Masking: None (Open Label)Primary Purpose: Other

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The study will take place in the ICU (Intensive Care Unit) or in the CICU (Cardiac Intensive Care Unit) units, on non-anaesthetized subjects with an arterial line inserted into the radial artery. Continuous recording will be performed in parallel using invasive arterial line recording and CardiacSen...

The study will take place in the ICU (Intensive Care Unit) or in the CICU (Cardiac Intensive Care Unit) units, on non-anaesthetized subjects with an arterial line inserted into the radial artery. Continuous recording will be performed in parallel using invasive arterial line recording and CardiacSenseBP1 non-invasive recording. The ECG data recorded in the ICU will also be obtained. . Up to 80 subjects will be included in the study. The subject will possibly be connected to the CardiacSense1BP device a few times to check repeatability. The first measurement will be of up to 24h. Subsequent measurements will be of up to 5h. Data analysis will be performed offline. Data is collected for CardiacSense1BP device algorithm development.

Tracking Information

NCT #
NCT04215185
Collaborators
Not Provided
Investigators
Principal Investigator: Adi Nimrod, Dr. Director Intensive care unit, Tel-Aviv Sourasky Medical Center