Sleep Apnea : Diagnosis and Monitoring

NCT03571477 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 45

Last updated 2019-01-04

No results posted yet for this study

Summary

This prospective study aims to evaluate a new medical screening method to detect and discriminate sleep apnea-hypopnea events. A new device called ApneaBand will be tested to propose a new screening method facilitating the diagnosis and monitoring of the sleep apnea syndrom, still underdiagnosed. This device will be tested in comparison with polysomnography (PSG), the gold standard reference method of sleep apnea diagnosis.

Conditions

Interventions

DEVICE

ApneaBand

Mesure of oxygen saturation (oximetry), pulse wave (photoplethysmography), electrodermal activity and movements (tri-axial accelerometer)

Sponsors & Collaborators

  • Commissariat A L'energie Atomique

    collaborator OTHER_GOV
  • AIRFAN

    collaborator UNKNOWN
  • AGIR à Dom

    collaborator OTHER
  • University Hospital, Grenoble

    lead OTHER

Principal Investigators

  • Jean-Louis PEPIN, Pr · CHU Grenoble Alpes

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-06-15
Primary Completion
2018-12-17
Completion
2018-12-17

Countries

  • France

Study Locations

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Entities

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 NCT03571477 on ClinicalTrials.gov