Diagnosing Sleep Apnoea with Implantable Continuous Monitoring: The Reveal LinQ Sleep Apnoea Algorithm

Not Applicable

• Conditions: Obstructive Sleep Apnoea; Respiratory - Sleep apnoea; Cardiovascular - Other cardiovascular diseases

• Registration Number: ACTRN12620000368932
• Lead Sponsor: niversity of Adelaide

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-03-17
• Last Update Posted: 23 March 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

This study will recruit patients with an implantable Medtronic LinQ device for clinically indicated reasons

Exclusion Criteria

1.Contraindication to intracardiac monitor implantation
2.Contraindication to undergoing overnight sleep study
3.Inability to provide informed consent

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Diagnosis of obstructive sleep apnoea based on a variety of algorithms using data extracted from implantable Medtronic LinQ device.<br><br>The algorithms will be retrospectively evaluated against the gold standard of the simultaneously undertaken polysomnography..[Immediately following sleep study.]