Impact of the Mandibular Advancement Device on Sleep Apnea During CPAP Withdrawal
Recruiting
N/A
Interventional Study
Sleep Apnea, Obstructive
Endothelial Dysfunction
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 75
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 40 (estimated)
- Sponsor
- University Hospital, Angers · Government
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About This Trial
Obstructive sleep apnea hypopnea syndrome (OSAS) is a frequent disease with neuropsychological and cardiovascular (CV) consequences. Continuous positive pressure (CPAP), the main treatment for OSAHS, is effective on the majority of symptoms but restrictive, which can promote non-compliance. Treatment interruptions are often observed in connection with intercurrent events such as nasal obstructions…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patient accepting MAD treatment
* Patient with an apnea-hypopnea index (AHI) greater than 15 events per hour on the initial recording
* Patient with excessive daytime sleepiness during initial treatment (ESE\>10)
* Patient treated for more than 12 months by CPAP with average c…
Contacts