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Feasibility of a Sensor-less Sleep Monitor (Somnofy®) in Diagnosis and Follow-up in Obstructive Sleep Apnea.

NCT05049135 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 65

Last updated 2023-03-20

No results posted yet for this study

Summary

To evaluate the feasibility of a sensor-less sleep monitor (Somnofy®) in diagnosis and follow-up in obstructive sleep apnea. The study will explore the monitor's usefulness in detection of apnea during sleep, and compare the data to standard diagnostic registrations.

Conditions

Interventions

DEVICE

Somnofy® sleep monitor

Registration of sleep score and apneas with radar sensor technology at time of primary investigation and 12 weeks after treatment initiation with continuous positive airway pressure (CPAP)

Sponsors & Collaborators

  • Norwegian University of Science and Technology

    collaborator OTHER

  • VitalThings

    collaborator INDUSTRY

  • Helse Nord-Trøndelag HF

    lead OTHER

Principal Investigators

  • Øystein Risa, PhD · NTNU, Fac of Med and Health Sci, Dept of Circulation and Medical Imaging

  • Carl Platou, MD · North Trøndelag Hospital Trust

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2022-12-31
Completion
2023-03-07

Countries

  • Norway

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 NCT05049135 on ClinicalTrials.gov