MedPath

Early Sleep Apnea Termination Using Sound Stimulation

Not Applicable
Completed
Conditions
Sleep Apnea
Interventions
Other: Sound stimulation
Registration Number
NCT03753971
Lead Sponsor
Raphael Heinzer
Brief Summary

Current evidence suggest that sleep apnea-associated oxygen desaturations may induce cardiovascular morbidities in the long term, whereas arousals associated with sleep apneas seem to induce mainly transient nocturnal hypertension. Reducing the occurrence and the magnitude of sleep apnea-associated oxygen desaturations could therefore have a beneficial effect on sleep apnea-associated comobidities. Since sleep apneas usually end with an arousal allowing pharyngeal muscles reactivation, a treatment option could consist of generating an early short awakening to anticipate apnea termination and decrease the risk of oxygen desaturation. The aim of this study is thus to determine if an early sleep apnea termination through the emission of a sound can achieve lower oxygen desaturations compared with "untreated" sleep apneas.

Detailed Description

The aim of the study is to determine the effect of short sound stimulations on sleep apnea associated desaturations

20 OSA subjects will be recruited and studied with polysomnography and a head band allowing to emit short sound stimulations during sleep. the study will take nplace at the Center for investigation and research in sleep (CIRS)

The magnitude of oxygen desaturations following apnea with and without sound stimulations will be compared. The effects of different types of sound stimulations on the magnitude of cortical and autonomic reactions will also be studied as well as the patients' subjective perception of the sounds.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
8
Inclusion Criteria
  • Age > 18 years
  • Able to give informed consent as documented by signature
  • Apnea / hypopnea index > 30 / h (severe)
  • Obstructive Apnea Index > 15 / h
  • Mean amplitude of desaturations (during diagnostic night) ≥ 5%
Exclusion Criteria
  • Perception deafness
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.,
  • Professional drivers

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Apneas with and without interventionSound stimulationEach patient will be his own control.
Primary Outcome Measures
NameTimeMethod
Differences in sleep apnea associted oxygen desaturationsDuring the polysomnography night

Differences in the magnitude of blood oxygen desaturation between treated and untreated sleep apnea events (in % of SaO2)

Secondary Outcome Measures
NameTimeMethod
Percentage of sound stimulations associated with autonomic arousals (%)During the polysomnography night

Autonomic arousals will be assessed by pulse wave amplitude variations

Duration of the apnea (seconds)During the polysomnography night

Duration of breathing cessation assessed by nasal cannula (in seconds)

Magnitude of autonomic reactions (% of pulse wave amplitude drop)During the polysomnography night

Magnitude (% of baseline) of pulse wave amplitude drop following different types of sound stimulations

Percentage of sound stimulations associated with cortical and subcortical arousals (%)During the polysomnography night

Each arousal will be assessed using the polysomnography EEG

Magnitude of autonomic reactions (duration of pulse wave amplitude drop)During the polysomnography night

Duration of pulse wave amplitude drop following different types of sound stimulations (in seconds)

Duration of EEG arousals (in seconds)During the polysomnography night

Duration (in seconds) of EEG arousals following different types of sound stimulations

Trial Locations

Locations (1)

Adrien Waeber

🇨🇭

Jouxtens-Mézery, Vaud, Switzerland

© Copyright 2025. All Rights Reserved by MedPath