Validation of a Contactless Vital Signs Measurement Sensor

Status Completed

Clinical Trial Summary

The primary aim of this study is to validate the performance of Sleepiz One+ for the measurement of vital physiological parameters in adult population, against a laboratory-based polysomnography. Additionally, the investigators will evaluate Sleepiz One+ ability to identify patients with a high risk of suffering from a sleep-related breathing disorder based on apnea-hypopnea index estimation. Participants will undergo measurement with Sleepiz One+ and a polysomnography device while resting in bed for 20 min as well as during sleep for the duration of the following night.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04676191
Study type	Interventional
Source	Sleepiz AG
Contact
Status	Completed
Phase	N/A
Start date	September 10, 2020
Completion date	January 12, 2022

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