JPRN-UMIN000023319尚未招募3 期
on-randomized, single-center study for efficacy and safety of telemonitoring in the continuous positive airway pressure treatment for patient with newly diagnosed sleep apnea syndrome - Telemonitoring study of CPAP for SAS
Inoue Hospital0 个研究点目标入组 60 人开始时间: 2016年7月25日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 ot applicable(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •Patients who meet one of the following criteria are excluded. 1. Patients with predominant central sleep apnea (CSA) 2. Patients with severe heart failure 3. Patient with severe respiratory failure 4. Patient with dementia 5. Patients with severe sleep disorder except SAS 6. Patients who some significant disease which influences CPAP therapy 7. Patients with claustrophobia 8. Patients who has past history of CPAP therapy. 9. Patients who want to be treated with oral appliance 10. Patients with significant nasal obstruction. 11. Occupational bus, truck, and taxi drivers who are screened by regular check-up, diagnosed as SAS, and introduced CPAP treatment. 12. Patient who sleeps without intending 13. Patients who cannot be contacted by telephone or e-mail regularly 14. Patients who participated in the other clinical study in last four months 15. Patients who are regularly visit our hospital with interval shorter than 3 months 16. Patients who are assessed as inadequate as the object of this clinical study by principal investigator
研究者
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