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.
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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