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临床试验/ACTRN12614001202651
ACTRN12614001202651已完成未知

Can continuous positive airway pressure treatment of patients with moderate obstructive sleep apnoea prevent sleep apnoea-related brain damage?

Dr. Carrie Innes0 个研究点目标入组 45 人开始时间: 2014年11月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
45

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Prevention
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
All

入选标准

  • All participants:
  • Be at least 18 yrs but no older than 80 yrs.
  • Normal time to bed between the hours of 0900 pm and 1200 am.
  • Normal time in bed of 7 to 9 hours.
  • Have a basic ability in English (verbal and written).
  • Participants with moderate OSA:
  • Be diagnosed with moderate OSA (15 - 29 OSA-related events per hour during Level 2 Sleep Study.
  • Participants without OSA:
  • Have <10 OSA-related events per hour during Level 2 Sleep Study.

排除标准

  • Currently receiving or previously received OSA treatment.
  • A history of physiological, psychiatric, or neurological disorders that could affect or is affecting sleep behaviour, fatigue, cerebral perfusion or brain structure (e.g. chronic obstructive pulmonary disease, congestive heart disease, diabetes, heart failure, hypertension > 150/90, migraine, myocardial infarction, stroke, previous brain surgery, stroke, traumatic brain injury, etc., but not mild depression).
  • Currently taking any medication that could impact on cerebral perfusion (e.g., ACE inhibitors, nitrates …).
  • Not willing or unable to give consent.
  • Not willing or unable to remove metal that could either be harmful to the participant during a MRI or could likely create MRI artefacts that negatively affect the quality of the scan.
  • Based on current Sleep Unit criteria, not have any reason for urgent treatment.

研究者

发起方
Dr. Carrie Innes

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