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.
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Fondation Bon Sauveur / cabinet médical / cabinet dentaire, Albi, France
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
Primary outcomes
-
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
-
Percentage of patients with AHI reduced by at least 50% compared to baseline measured by PG/PSG
Time frame: 3 months and 2 years
-
Percentage of patients who no longer suffer from severe daytime sleepiness (Epworth Sleepiness scale)
Time frame: 3 months, 2 years and 5 years
-
Sleep quality of life (Quebec Sleep Questionaire)
Time frame: 3 months, 2 years and 5 years
-
Percentage of patients who stopped the therapy for dento-maxillofacial side effects
Time frame: 6 months, 1, 2, 3, 4 and 5 years
-
Percentage of patients with satisfactory compliance
Time frame: 3 months, 2 and 5 years.
-
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.
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