Validation of a new method for ambulant diagnosis of sleep related breathing disorders using body sound.

• Conditions: G47.3; Sleep apnoea

• Registration Number: DRKS00011195
• Lead Sponsor: niversitätsklinikum Ulm

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-10-18
• Study Completion: 2018-04-02
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Signed consent
• Suspected sleep-related breathing disorder

Exclusion Criteria

• known allergies or intolerances with patches
• serious illnesses or diseases that affect the participation of the subjects in the study or make them impossible
• Lack of willingness to participate in the study

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The aim of this study is to verify if the new sleep monitor (body sound) is equivalent to polysomnography in the diagnosis of sleep-related respiratory disorders.

Secondary Outcome Measures

Name	Time	Method
The secondary aim of this study is to verify if the new sleep monitor can be used reliably and without any complications. Another secondary aim of this study is to examine if there are other correlations between the data of the new sleep monitor (e.g. heart sounds and respiratory sounds) and PSG (e.g. ECG and respiratory flow).