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临床试验/NCT00243139
NCT00243139已完成2 期

A Randomized Controlled Trial of a Mandibular Advancement Device for Obstructive Sleep Apnea

Nykøbing Falster County Hospital2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 1999年7月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
90
试验地点
2
主要终点
Change in sleep parameters, especially apnea-hypopnea index (AHI).

研究概览

简要总结

The purpose of this study was to determine how effective a custom-made standard dental splint (activator) advancing the lower jaw forward is in treatment of obstructive sleep apnea, and further to find factors for identification of those patients likely to benefit from this treatment.

详细描述

Obstructive sleep apnea (OSA) is far the most common sleep disordered breathing, affecting 2-4% of the adult population. The repetitive obstructions are located in the pharyngeal airway, leading to sleep fragmentation and resulting in excessive daytime sleepiness with consequences for ability to work, road safety and quality of life. Furthermore, OSA is an independant riskfactor for cardiovascular disease. The treatment of choice today is continuous positive airway pressure (CPAP) but a main problem with CPAP is an unsatisfactory compliance. An alternative conservative more user-friendly treatment could be oral appliances, intending to increase the pharyngeal airway directly by tongue retaining devices or indirectly by mandibular advancing devices. Though several randomized studies on oral appliances have come recent years, all giving some evidence for effect on OSA, they all had some shortcomings, such as using crossover design, small sample sizes, under-reporting of methods and data and lack of blinding.

In this study of a mandibular advancement device was used a parallel group design with an inactive device and no intervention as controls. Beside the effect on sleep, daytime sleepiness and quality of life, the study aimed to find objective factors to be used as predictors of the outcome.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • AHI > 5 on polysomnography
  • sufficient set of teeth to hold a splint
  • written informed consent

排除标准

  • sleep apnea with severe cardiovascular disease
  • other severe somatic or psychiatric disease
  • periodontal disease
  • significant occlusal dysfunction
  • pregnant women

结局指标

主要结局

Change in sleep parameters, especially apnea-hypopnea index (AHI).

次要结局

  • Change in daytime sleepiness, assessed by Epworth Sleepiness Scale.
  • Change in quality of life, assessed by SF-36.

研究者

发起方
Nykøbing Falster County Hospital
申办方类型
Other

研究点 (2)

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