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Study identifier: NCT03924817 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Registry Study on Prescription, Patient Pathways, Therapy Efficacy and Usage of Mandibular Advancement Devices in Obstructive Sleep Apnea - PATT-OSA Registry

Condition: Obstructive Sleep Apnea  ·  Sponsor: ResMed

PhaseN/A
Planned participants500
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

During sleep, the muscle tonus in the oropharyngeal space is lost, the tongue might fall back andthe volume of the pharynx decreases. Air cannot pass through as it would in the awake state and thus airflow limitations occur. The person asleep might compensate the flow limitation by breathing faster, which causes the soft tissue to vibrate (= snoring). Further narrowing of the airways can lead to obstructive apneas (complete airway collapse and stopping of airflow). First line therapy for obstructive sleep apnea (OSA) is positive airway pressure (PAP) that keeps the airways open with a pneumatic splint. Since PAP involves wearing a facial mask that applies air pressure into the airways, some patients cannot tolerate this therapy. These patients might be candidates for an alternative treatment approach with a mandibular advancement device (MAD).

This description comes directly from the study's public registry record.

Talk to the study team

Oliver Munt, PhD  ·  +491629056360  ·  oliver.munt@resmed.de

Always discuss trial participation with your own doctor first.

Locations (4)

Schlaf- und Beatmungszentrum BlaubeurenBlaubeuren Abbey, Badden-Württemberg, GermanyNot Yet Recruiting
Ruhrlandklinik EssenEssen, North Rhine-Westphalia, GermanyRecruiting
Zentrum für Schlafmedizin Dr. WarmuthBerlin, GermanyNot Yet Recruiting
Universitätsklinikum Regensburg - Klinik für Innere Medizin IIRegensburg, GermanyNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT03924817