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NCT05056766: OAMMM

How Does the Clinical and Paraclinical Efficacy of an Oral Appliance Evolved According to Propulsion: Control With Each mm of Advancement

Completed Last updated 8 September 2025
What this trial tests

trial testing questionnaires: Epworth Sleepiness Scale; Pichot fatigue questionnaire. in Sleep Apnea Syndromes in 20 participants. Completed in 1 September 2022.

Timeline
1 September 2021
Primary endpoint
1 September 2022
1 September 2022

Quick facts

Lead sponsorCentre Hospitalier de Valence
StatusCompleted
Study typeOBSERVATIONAL
Enrollment20
Start date1 September 2021
Primary completion1 September 2022
Estimated completion1 September 2022
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Centre Hospitalier de Valence

Who can join

18 and older, any sex, with Sleep Apnea Syndromes or Sleep Apnea, Obstructive. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The OAMMM study is a mono-centrer , non interventional, prospective study, carried out in CH Valence Oral Appliance is indicated for first line moderate sleep Apnea Syndrome or severe sleep Apnea Syndrome after failure of positive airway pressure (CPAP). Clinical impact of each mm advancement of Oral Appliance is imperfectly assessed. The study aim to assess clinical and paraclinical efficacy of an oral Appliance on each mm of advancement.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Sleep Apnea Syndromes

Currently open trials in the same condition.

Other Centre Hospitalier de Valence trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05056766.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing