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临床试验/NCT02677168
NCT02677168已完成不适用

Continuous Negative External Pressure (cNEP) for the Treatment of Obstructive Sleep Apnea (OSA)

Sommetrics, Inc.2 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2016年5月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
71
试验地点
2
主要终点
"Sustained Response" of reduction of AHI (apnea hypopnea index) at PSG (polysomnography) II

研究概览

简要总结

The purpose of this study is to determine whether cNEP (continuous positive external pressure) is effective in treating obstructive sleep apnea

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • PSG performed within the previous twelve months that documents the presence of obstructive sleep apnea (the "qualifying PSG")
  • on that PSG, AHI must be 10 - 50/hr and >80% of the apneas and hypopneas must be obstructive
  • no significant changes in health, medications, or lifestyle since the qualifying PSG

排除标准

  • previous major surgery, injury or radiation to the neck
  • beard or excessive hair on the area of the neck where the collar will be applied
  • carotid artery disease
  • serious medical conditions
  • pregnancy
  • use of home oxygen
  • silicone allergy
  • sleep disturbance other than obstructive sleep apnea

研究组 & 干预措施

cNEP

Experimental

Subjects with OSA will be treated with cNEP (continuous negative external pressure) at home for three weeks

干预措施: cNEP (Device)

结局指标

主要结局

"Sustained Response" of reduction of AHI (apnea hypopnea index) at PSG (polysomnography) II

时间窗: three weeks--PSG II will be done after three weeks of home use of cNEP following PSG I

A response (either initial or sustained) is defined as an AHI that is \< 50% of the qualifying PSG (polysomnography) that is also \< 15/hr

occurrence of adverse events

时间窗: three weeks

Adverse events that occur during the three weeks of cNEP home use.

次要结局

  • time of SpO2 (oxygen saturation) < 90%(during each of the overnight PSGs)
  • Three CGI (clinical global impression) subjective measures(three weeks after the initiation of home cNEP)
  • "Initial Response" of AHI at PSG I(up to 12 months after the qualifying PSG)
  • Comparison of AHI at PSG I and PSG II(three weeks)
  • hours of home use of cNEP per night(three weeks after initiation of home cNEP)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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