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Contactless Detection of Sleep Apnea

NCT04670848 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 116

Last updated 2022-01-25

No results posted yet for this study

Summary

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.

Conditions

Interventions

DEVICE

Sleepiz One+ vs. polysomnography

Simultaneous sleep recording with polysomnography and Sleepiz One+ device

Sponsors & Collaborators

  • Sleepiz AG

    lead INDUSTRY

Principal Investigators

  • Christoph Schöbel, Prof. Dr. med. · Universitätsmedizin Essen Ruhrlandklinik

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-12-07
Primary Completion
2021-12-21
Completion
2021-12-21

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04670848 on ClinicalTrials.gov