Skip to main content
OpenTrials
Completed

NCT Number: NCT01326143

Narval CC Mandibular Repositioning Device in the Second-line Treatment of Severe Obstructive Sleep Apnea Hypopnea (OSAH)

The purpose of this study is to evaluate the long-term efficacy, tolerance and compliance of ORM Narval Mandibular Repositioning Device (MRD) as a second-line treatment for patients with severe Obstructive Sleep Apnea Hypopnea (OSAH) syndrome who refuse or are intolerant to Continuous Positive Airway Pressure (CPAP) treatment.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Fondation Bon Sauveur / cabinet médical / cabinet dentaire, Albi, France

Loading trial locations.

About this study

OSAH is a common condition which occurs in between 1 and 4% of the adult population. Respiratory obstruction may be complete (apnea) or incomplete (hypopnea). This disorder disturbs the architecture and quality of sleep, and is a known risk factor in the development of cardiovascular and metabolic diseases. CPAP is the standard treatment, however in some cases patients are unable to use it (rejection, intolerance, etc.). In such circumstances, treatment using a MRD may result in an improvement of symptoms.

Very few long-term clinical data are available on treatment of OSAH by MRD. This study should allow to have a precise and representative vision of 5 years results of ORM Narval MRD treatment in conditions of good practices (titration, controls of efficacy).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patient with severe OSAH (AHI > 30 or AHI of between 5 and 30 along with severe daytime sleepiness),
  • intolerant to or having refused CPAP therapy,
  • no dental, parodontal or articulatory contraindications,
  • no experience of any mandibular advancement device therapy,
  • medical insurance.

Exclusion criteria

  • severe psychiatric disorders or severe neuromuscular disorders
  • > 20% of central apneas during the baseline assessment,
  • severe OSAH with an AHI > 30 associated with another sleep pathology (narcolepsy with or without cataplexy, idiopathic hypersomnia, severe restless legs syndrome),
  • pregnant or breastfeeding woman,
  • Informed consent not signed,
  • patient requiring special protection such as patients with appointed guardians and patients without legal or administrative rights,
  • patient who is completely or partially edentulous

Treatment and study plan

ORM Narval MRD

Device

Primary outcomes

  1. Percentage of patients with Apnea/Hypopnea Index (AHI) reduced by at least 50% compared to baseline measured by Polygraphy/Polysomnography (PG/PSG)

    Time frame: 5 years

Secondary outcomes

  1. Percentage of patients with AHI reduced by at least 50% compared to baseline measured by PG/PSG

    Time frame: 3 months and 2 years

  2. Percentage of patients who no longer suffer from severe daytime sleepiness (Epworth Sleepiness scale)

    Time frame: 3 months, 2 years and 5 years

  3. Sleep quality of life (Quebec Sleep Questionaire)

    Time frame: 3 months, 2 years and 5 years

  4. Percentage of patients who stopped the therapy for dento-maxillofacial side effects

    Time frame: 6 months, 1, 2, 3, 4 and 5 years

  5. Percentage of patients with satisfactory compliance

    Time frame: 3 months, 2 and 5 years.

  6. Fatigue score (Pichot questionaire)

    Time frame: 3 months, 2 and 5 years

Sponsors and collaborators

Lead sponsor

ResMed

Industry

Registry information

Official study title

ORM Narval Mandibular Repositioning Device in the Second-line Treatment of Severe OSAH

Acronym: ORCADES

Important dates

Study start
2011
Primary completion
2019
Study completion
2019
First posted
Mar 30, 2011
Registry last updated
Apr 2, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.