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Comparison of Two Reeducation Methods in Children With Persistent Sleep Apnea, a Randomize

Myofunctional therapy has been shown to be effectively reduce symptoms of paediatric obstructive sleep apnea, usually performed after adenotonsillectomy. This study aims to evaluate the effectiveness of Passive Oral Myofunctional Reeducation (using a flexible oral appliance) compared to nasal hygiene alone (control gro

Condition(s)Obstructive Sleep Apnea of Child, Sleep-Disordered Breathing, Adenotonsillar Hypertrophy
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryMyofunctional therapy has been shown to be effectively reduce symptoms of paediatric obstructive sleep apnea, usually performed after adenotonsillectomy. This study aims to evaluate the effectiveness of Passive Oral Myofunctional Reeducation (using a flexible oral appliance) compared to nasal hygiene alone (control group), in a population of children scheduled for adenotonsillectomy.
Who can participateInclusion Criteria: participants must: * present signs of obstructive sleep apnea: snoring, apnea / respiratory pauses audible by the entourage (objectivized by a score, to the Pediatric Sleep Questionnaire (PSQ) , greater than or equal to 0.33- This questionnaire comprises twenty-two Questions and has a good sensitivity (83%) and specificity (87%) in screening for pediatric sleep apnea. * be programmed for adenoidectomy, tonsillectomy or adeno-tonsillectomy within 3 months (or more). Exclusion Criteria: participants should not: * present with a craniofacial syndrome nor a severe medical condition with complex medical management, * present with an abnormality of the neuromuscular tone (such as Duchenne myopathy or cerebral palsy) * receive orthodontic therapy during the study * have a clas
Ages4 Years to 14 Years
SexAll
Lead sponsorUniversité de Montréal
LocationsMontreal, Quebec, Canada
Start date2024-03-20
NCT IDNCT06634264
Official listinghttps://clinicaltrials.gov/study/NCT06634264

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