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Data Collection From the CardiacSense1 and Other Modalities for Developing a System for Monitoring of Respiratory Rate — RRP  

Respiratory Disease Clinical Trial

Official title:
Anonymized Data Collection From the CardiacSense1 and Other Modalities for the Purpose of Developing a System for Monitoring of Respiratory Rate

Clinical Trial Summary

Collect data from the CardiacSense1's sensors and Capnograph, for the purpose of developing a wearable system for monitoring of Respiratory Rate (RR) in patients while at hospital

Clinical Trial Description

Hospitalized subjects, diagnosed with a Respiratory disease or subjects with no known Respiratory disease will be will be connected simultaneously to CardiacSense watch and Capnograph for a duration of at least 30 minutes and up to 24 hours in order to collect data for the purpose of developing a wearable system for monitoring of Respiratory Rate (RR) by the CardiacSense watch. The CardiacSense1 is a wrist worn device designed to detect atrial fibrillation. CardiacSense1 senses the radial artery inflation and deflation and together with a PPG sensors give an ultimate performance that is superior to PPG only. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04580615
Study type Interventional
Source CardiacSense Ltd.
Contact
Status Active, not recruiting
Phase N/A
Start date June 3, 2020
Completion date May 1, 2022
View Details
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