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Evaluation of ApneaLink Plus Scoring Capabilities

NCT00823134 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2020-05-12

Study results available
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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

Conditions

  • Sleep Apnea, Central
  • Sleep Apnea, Obstructive

Interventions

DEVICE

ApneaLink Plus

Device used to evaluate for the presence of obstructive, central or mixed apneas

Sponsors & Collaborators

  • ResMed

    lead INDUSTRY

Principal Investigators

  • Knut Joechle, PhD · ResMed

  • Heribert Knape, MD · Medizinische Klinik für Atemwegserkrankungen und Allergien, Fachkliniken Wangen

Study Design

Allocation
NA
Purpose
SCREENING
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2009-03-31
Completion
2009-03-31

Countries

  • Germany

Study Locations

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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 NCT00823134 on ClinicalTrials.gov