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临床试验/NCT02535234
NCT02535234已完成不适用

Comparison of the Subjective and Objective Performance of a Novel Continuous Positive Airway Pressure (CPAP) System With a Traditional Continuous Positive Airway Pressure (CPAP) System.

ResMed2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2016年4月最近更新:
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
30
试验地点
2
主要终点
Subjective usability ratings of the prototype system using a visual analogue scale, compared to a reference level and the second full system.

研究概览

简要总结

Randomised crossover trial of a novel and traditional Continuous Positive Airway Pressure (CPAP) system in Obstructive Sleep Apnoea patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Subjective usability ratings of the prototype system using a visual analogue scale, compared to a reference level and the second full system.

时间窗: 1 year

Participants will be asked to complete a short questionnaire at the end of each week to evaluate the general usability of the system. The questionnaire will include questions related to system use and comfort. The participants will answer the questions using an 11-point Likert scale.

次要结局

未报告次要终点

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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