Contactless Detection of Sleep Apnea

  • days left to enroll
  • participants needed
  • sponsor
    Sleepiz AG
Updated on 3 February 2021


In this study the inestigators aim to validate the performance of Sleepiz One+ for sleep apnea detection during routine diagnostic sleep studies. Patients who are prescribed polysomnography study will be asked to participate and undergo a simultaneous sleep recording with radar sensor-based device.

Condition Sleep apnea, Sleep Apnea Syndromes
Treatment Sleepiz One+ vs. polysomnography
Clinical Study IdentifierNCT04670848
SponsorSleepiz AG
Last Modified on3 February 2021


Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Sleep apnea or Sleep Apnea Syndromes?
Age >18years
Ability and consent to undergo electrophysiological routine assessment
Patients suspected to suffer from sleep apnea or any other sleep related disorder

Exclusion Criteria

Previous enrollment into the current study
Enrollment of the investigator, his/her family members and other dependent persons
Cardiac pacemaker or another implanted electrical device
Women who are pregnant or breastfeeding
Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, delirium etc. of the participant
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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