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Clinical Trials/NCT03267927
NCT03267927
Completed
Not Applicable

Management of Obstructive Sleep Apnea (OSA) in Children and Maxillary and Mandibular Development

Rennes University Hospital1 site in 1 country4 target enrollmentNovember 5, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obstructive Sleep Apnea Syndrome
Sponsor
Rennes University Hospital
Enrollment
4
Locations
1
Primary Endpoint
Assessment in 5 to 7 year-old children the efficacy on OSA (removal or decrease of apnea/hypopnea) of Rapid Palatal Expansion combined with advancement using a mandibular advancement appliance (MGA™)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Assessment of the association of maxillary expansion using a rapid palatal expansion, use of a mandibular advancement appliance (MGA™) and of a device allowing sleep in a semi-seated position (Yoobreath™) in patients with Obstructive Sleep Apnea (OAS). MGA™ and YooBreath™ constitute the Yookid system™.

Detailed Description

Obstructive Sleep Apnea syndrome (OSA) shows a 10% morbidity rate in children with a higher rate between the ages of 3 and 5. Generally speaking, its prevalence is underestimated. Furthermore, detecting OSA remains difficult due to its particular physiopathology. The decrease in nasopharyngeal airway dimensions is the most common etiology. This decrease is related to soft tissues as well as maxillomandibular abnormalities. The aim of the study is to show that reducing sleep apnea in children remains possible when inducing rapid palatal expansion and mandibular advancement using the Yookid™ system. The Yookid™ system associates a mandibular advancement appliance and repositioning of the patient during sleep.

Registry
clinicaltrials.gov
Start Date
November 5, 2017
End Date
March 25, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Rennes University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 5 to 7 year-old children
  • Children with American Society of Anesthesiologists score (ASA) of 1 and 2
  • Children with signs of OSA during examination and clinical exam
  • Children with apnea-hypopnea index (AHI) from 1 to 5 (one to five sleep apnea / hour during PSG)
  • Children with a class II division 1 angle malocclusion (at the canines level rotation center) and skeletal class II according to Delaire analysis

Exclusion Criteria

  • OSA associated to syndromic disorder and/or syndrome
  • Body/Mass Index (BMI) \> 97ème percentile according to development curves (obese children)
  • Central sleep apnea
  • Respiratory allergy
  • Previous ear, nose and throat (ENT) surgery
  • Hypertrophic tonsils needing surgery
  • Adenoid hypertrophy needing surgery
  • Patients with ankyloglossia

Outcomes

Primary Outcomes

Assessment in 5 to 7 year-old children the efficacy on OSA (removal or decrease of apnea/hypopnea) of Rapid Palatal Expansion combined with advancement using a mandibular advancement appliance (MGA™)

Time Frame: Day 180

Assessment in 5 to 7 year-old children the efficacy on OSA (removal or decrease of apnea/hypopnea) of Rapid Palatal Expansion combined with a device allowing a semi-seated sleeping position (YooBreath™)

Time Frame: Day 180

Secondary Outcomes

  • Assessment of quality of wakefulness(Day 180)
  • Sleep improvement(Day -7, day 180)
  • Assessment of quality of sleep(Day 180)
  • Measurement of lengthening of mandibular body and ramus(Day -7, day 180)
  • Assessment of intensity of dental pain the morning on waking after using the MGA™ system(Day 60, day 90, day 120, day 150, day 180)
  • Assessment of salivary disorders the morning on waking after using the MGA™ system(Day 60, day 90, day 120, day 150, day 180)
  • Improvement of breathing(Day -7, day 180)
  • Assessment of dental occlusion(Day -7, day 180)
  • Assessement by the child and the parents of the treatment and the devices used(Day 180)
  • Assessment of the compliance(Day 0, day 15, day 60, day 90, day 120, day 150, day 180)
  • Assessment of intensity of pain during rapid palatal expansion(Day 60)
  • Assessment of duration of pain during rapid palatal expansion(Day 60)
  • Assessment of duration of dental pain the morning on waking after using the MGA™ system(Day 60, day 90, day 120, day 150, day 180)
  • Assessment of risk of falling using the Yoobreath system™(Day 15, day 60, day 90, day 120, day 150, day 180)
  • Assessment of pain related to the semi-seated position(Day 15, day 60, day 90, day 120, day 150, day 180)
  • Assessment of disorders in falling asleep and sleep quality (micro arousals)(Day 15, day 60, day 90, day 120, day 150, day 180)

Study Sites (1)

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