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临床试验/NCT03726346
NCT03726346已完成不适用

The Evaluation of the Toffee Mask for the Treatment of Obstructive Sleep Apnea

Fisher and Paykel Healthcare2 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2018年11月26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
入组人数
39
试验地点
2
主要终点
Toffee Mask Treatment Seal Performance-Subjective

研究概览

简要总结

This investigation is a prospective, non-randomized, non-blinded study. This investigation is designed to evaluate the performance, comfort and ease of use of the F&P Toffee mask amongst Obstructive Sleep Apnea (OSA) patients. Up to 45 OSA patients will be recruited from the Pulmonary Disease Specialists Research database.

详细描述

Visit 1 will involve the participants being consented into the trial. Visit 2 will involve the participants being fitted with the F&P Toffee mask for use in home. The participant will then come in to return the mask (Visit Three) and have a final interview, this ensures the maximum time participants will be exposed to the Toffee mask in home will be 14 ± 4 days from visit two. The mask will be returned to the Institution at the conclusion of the trial and the participant will return to their previous mask. The Institution will recruit all patients within 2 weeks of the beginning of the study.

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
22 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult (22+ years of age)
  • Able to give informed consent
  • Apnea hypopnea Index (AHI) ≥ 5 on diagnostic night
  • Either prescribed Automatic positive airway pressure (APAP), Continuous positive airway pressure (CPAP) or Bi-level positive airway pressure (PAP) for OSA
  • Fluent in spoken and written English
  • Existing OSA mask user

排除标准

  • Inability to give informed consent
  • Participant intolerant to PAP
  • Anatomical or physiological conditions making PAP therapy inappropriate
  • Current diagnosis of respiratory disease or carbon Dioxide (CO2) retention
  • Pregnant or may think they are pregnant.

结局指标

主要结局

Toffee Mask Treatment Seal Performance-Subjective

时间窗: 14±4 days in home

Sealing performance of Toffee mask determined from questionnaires - Subjective

Toffee Mask Acceptability

时间窗: 14±4 days in home

Participant preference for the Toffee mask over their usual mask. Determined from questionnaires -Subjective

Toffee Mask Comfort

时间窗: 14±4 days in home

Overall Toffee mask comfort determined from questionnaires-Subjective

次要结局

  • Toffee Mask Treatment Performance-Objective(14±4 days in home)

研究者

发起方
Fisher and Paykel Healthcare
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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