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临床试验/ACTRN12605000120673
ACTRN12605000120673已完成未知

A comparison of efficacy and tolerability using two portable sleep apnoea monitoring devices: nocturnal oximetry versus nasal airflow in the triage diagnosis and screening of obstructive sleep apnoea.

Woolcock Institute of Medical Research0 个研究点目标入组 193 人开始时间: 2005年8月10日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
193

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
21 Years 至 o limit(—)
性别
All

入选标准

  • 1.Subjects presenting to the sleep laboratory for assessment of obstructive sleep apnea
  • 2.Age = 21
  • 3.Able to give consent

排除标准

  • 1.Clinically significant co morbidity,
  • including any unstable cardiovascular, gastrointestinal, metabolic,
  • pulmonary (e.g., asthma, chronic obstructive pulmonary disease, etc), renal, neurological, hepatic,
  • hematologic, immunologic, endocrine, psychiatric illness and/or
  • neoplastic disease.
  • 2.Patients unable to apply the monitoring devices (e.g. severe hand
  • arthritis, neuromuscular disease).
  • 3.Shift workers
  • 4.Known underlying sleep disorder

研究者

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