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临床试验/NCT07658053
NCT07658053尚未招募不适用

Effects of a Pacifier on the Development of Obstructive Sleep Apnea and Its Repercussions in Infants With Down Syndrome

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年7月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
试验地点
1

研究概览

简要总结

Obstructive Sleep Apnea (OSA) is characterised by repetitive collapse of the upper airway during sleep, inducing breathing disturbances that can result in oxygen desaturation and frequent arousals. In children, OSA can have long-term consequences on the development and on the cardiovascular system.

Down Syndrome (DS) is a genetic disorder associated with intellectual disability and many comorbidities. The prevalence of OSA is particularly high in patients with DS, from infancy. In a recent study, OSA was diagnosed in 97% infants and early diagnosis and intervention from the age of 6 months was associated with better neurocognitive outcome at 3 years old. Therefore, there is a need to develop new strategies to prevent OSA early in infancy.

OSA can be linked to some orofacial abnormalities presented by patients with DS. Indeed, orofacial functions and structures ca play a crucial role in OSA. For example, nose breathing allows the tongue to act as a stimulator of the transverse maxillary growth during childhood, allowing the upper airway to develop properly.

The primary objective of the present study is to evaluate the effects of a pacifier used by infants with Down Syndrome (from the age of 1 months) on the severity of OSA at the age of 6 months, by comparing a group of infants with the pacifier vs a group of infants without the pacifier.

The main hypothesis is that infants who used the pacifier from 1 month- to 6 month-old will have lower OSA severity (estimated by the obstructive apnea hypopnea index on polysomnography (PSG)).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
23 Days 至 38 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Group 1 (infants with CURAPROX pacifier)
  • Age 1 month (±1 week)
  • Children diagnosed with free and homogeneous trisomy 21
  • For whom a consultation is planned at ~1 month in the department of genetics
  • Affiliated to a social security scheme
  • With informed consent of the 2 legal representatives
  • Group 2 (infants without CURAPROX pacifier)
  • Infants included in the OMF21 study (sponsored by HCL, n°ID-RCB 2025-A01900-49, approved by ethical committee Nord-Ouest IV on October 9th 2025)
  • With informed consent of the 2 legal representatives for re-use of the data

排除标准

  • Group 1 (infants with CURAPROX pacifier)
  • Diagnosed with mosaic trisomy 21
  • Born preterm (gestation age at birth <37 weeks)
  • Known allergy to silicone
  • Currently participating to an interventional study protocol implying an ongoing exclusion period from other studies
  • Group 2 (infants without CURAPROX pacifier) - Use of the CURAPROX pacifier for ≥1 month

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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