Mandibular Advancement Devices Tali® in Patients With Syndrome of Obstructive Sleep Apnea and Hypopneas

ONIRIS

Status: Completed

Conditions: Syndrome of Obstructive Sleep Apnea and Hypopneas

Treatments: Device: Mandibular Advancement Devices

Study type: Observational

Funder types: Industry

Identifiers

NCT02878629

OAM Tali®

Details and patient eligibility

About

The main objective is to evaluate middle term compliance (≥ 2 years) of the Mandibular Advancement Devices Tali® in patients with Syndrome of Obstructive Sleep Apnea and Hypopneas.

Enrollment: 254 patients

Sex: All

Ages: 18 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Patients > 18 years treated with Mandibular Advancement Device Tali® from at least 2 years and at the latest 5 years.
• Patients who agree to participate to the study.