CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 23 enrolled
Drug / intervention
ApneaLink Plusdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00823134
NCT00823134N/ACompleted
CompareCT.gov

Evaluation of ApneaLink Plus Scoring Capabilities

ResMed·interventional·Posted Jan 15, 2009·Updated May 12, 2020

In Brief

A clinical study evaluating ApneaLink Plus for Sleep Apnea, Central and Sleep Apnea, Obstructive. Completed, enrolled 23 participants across 1 site.

Detailed 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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSleep Apnea, Central, Sleep Apnea, Obstructive
CountriesGermany
Collaborators--

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedJan 15, 2009
Enrollment StartDec 1, 2008
Primary CompletionMar 1, 2009
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 17.5 years ago

Interventions

ApneaLink Plusdevice

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