Sleep Apnoea Syndrome Without Chronic Heart Failure

Completed

• Conditions: Sleep Apnoea Syndrome

• Registration Number: NCT01775241
• Lead Sponsor: RWTH Aachen University

Brief Summary

It is the objective of this study to collect scientific data of sleep apnoea syndrome patients´ cardiac and respiratory function by additional sensors.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-10
• Study First Submitted: 2013-01-22
• Study First Submitted QC: 2013-01-22
• Study First Posted: 2013-01-24
• Primary Completion: 2013-03
• Study Completion: 2013-03
• Status Verified: 2014-01
• Last Update Submitted: 2014-01-07
• Last Update Posted: 2014-01-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

• patients with supected sleep apnoea syndrome and scheduled diagnosis at a sleep laboratory
• male and female patients aged at least 18 years
• persons who understand and follow the instructions of the study staff
• singed informed consent

Exclusion Criteria

• persons being housed in an institution by court or governmental order
• pregnancy or breastfeeding
• patients who are not able to consent
• acute or chronic inflammations of the external and middle auditory canal
• abnormal anatomic proportionsof the external and middle auditory canal which are pathological or congenital, for example limitation of the auditory canal
• persons in a dependence or in an employment contract to the investigator
• participation in another study at the same time

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Data collection	1 night

Trial Locations

Locations (1)

Univeristy Hospital Aachen; 🇩🇪 Aachen, North Rhine Westfalia, Germany