NCT00823134

Evaluation of ApneaLink Plus Scoring Capabilities

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 23 (actual)
• Sponsor: ResMed · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to investigate the following topics: * Determine the accuracy of ApneaLink Plus in separating Apneas into Obstructive Apneas, Mixed Apneas and Central Apneas. * Determine the accuracy of ApneaLink Plus in scoring Hypopneas according to the 2008 guidelines of the AASM = American Academy of Sleep Medcine. * Determine whether patients can start and stop the recorder and are able to attach the additional effort sensor by themselves using the patient instruction sheet

Detailed description

* Determine the accuracy of ApneaLink Plus in separating Apneas into Obstructive Apneas, Mixed Apneas and Central Apneas. * Determine the accuracy of ApneaLink Plus in scoring Hypopneas according to the 2008 guidelines of the AASM = American Academy of Sleep Medcine. * Determine whether patients can start and stop the recorder and are able to attach the additional effort sensor by themselves using the patient instruction sheet

Conditions

• Sleep Apnea, Central
• Sleep Apnea, Obstructive

Interventions

Type	Name	Description
DEVICE	ApneaLink Plus	Device used to evaluate for the presence of obstructive, central or mixed apneas

Timeline

• Start date: 2008-12-01
• Primary completion: 2009-03-01
• Completion: 2009-03-01
• First posted: 2009-01-15
• Last updated: 2020-05-12
• Results posted: 2020-05-12

Locations

1 site across 1 country: Germany