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

NCT02348970 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 211

Last updated 2018-08-31

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

ONIRIS®

sleeping test

DEVICE

TALI

sleeping test

Sponsors & Collaborators

  • ONIRIS

    lead INDUSTRY

Principal Investigators

  • RAYMOND Nathalie, MD · Hôpital Bel Air

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2018-04-28
Completion
2018-04-28

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT02348970 on ClinicalTrials.gov