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Efficacy and Compliance of the Mandibular Advancement Devices ONIRIS® vs. Custom Made Devices — IRIS  

Obstructive Sleep Apnea Clinical Trial

Official title:
Multicenters, Randomised Clinical Trial, to Evaluate Efficacy and Compliance of Mandibular Advancement Devices ONIRIS® vs. Laboratory Devices TALI in Patients With Syndrome of Obstructive Sleep Apnea and Hypopneas

Clinical Trial Summary

To evaluate the efficacy (non-inferiority) in terms of response between patients using custom fitted mandibular advancement devices ONIRIS® and patient using laboratory custom made devices TALI, after 2 months of use. Sleeping tests were performed.

Clinical Trial Description

Open, non-inferiority, controlled and rndomised clinical trial. Six months of inclusion. Each included patient will be followed during 12 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02348970
Study type Interventional
Source ONIRIS
Contact
Status Completed
Phase N/A
Start date January 2015
Completion date April 28, 2018
View Details
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