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临床试验/NCT03201055
NCT03201055已完成不适用

Assessment of Performance, Usability and Acceptance of a Continuous Positive Airway Pressure System to Alleviate Self-reported Snore in Non-apnoeic Participants

ResMed2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2017年10月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
ResMed
入组人数
24
试验地点
2
主要终点
Subjectively assess the participant and bed partner acceptability and usability of Snore PAP system

研究概览

简要总结

This study will aim to assess the acceptance of the Snore PAP system as a treatment concept for snore. The study will subjectively assess participant and bed partner acceptability and usability of the Snore PAP system and objectively assess participant compliance with the Snore PAP system.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Subjectively assess the participant and bed partner acceptability and usability of Snore PAP system

时间窗: 28 Nights

Subjective assessment will be assessed using the Likert scale using a 0-10 scale. With 0 being very negative and 10 being very positive.

次要结局

  • Objectively assess participant compliance with the Snore PAP system(28 Nights)
  • Subjectively assess the performance of the Snore PAP system in relieving: self-reported and bed partner reported snore in non-apnoeic participants.(28 Nights)

研究者

发起方
ResMed
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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Snore Positive Airway Pressure Trial | 临床试验