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临床试验/JPRN-UMIN000027645
JPRN-UMIN000027645已完成未知

Clinical study about the safety of Orexin receptor antagonist Suvorexant for severe sleep apnea syndrome - Clinical study about the safety of Orexin receptor antagonist Suvorexant for severe sleep apnea syndrome

Fujita Health University respiratory medicine department0 个研究点目标入组 30 人开始时间: 2017年6月5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
30

研究概览

简要总结

There is no significant difference in AHI (median: 48.3 times/hour on the first night, 50.2 times/hour on the second night p=0.58). Among the secondary endpoints, significant differences were found in sleep efficiency (median: 82.8% on first night, 87.8% on second night, p=0.004), REM sleep rate (median: 15.0% on first night, 21.2% on second night, p<0.001). There was no significant difference in the AHI of patients with severe sleep apnea before and after taking Suvorexant.

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

  • The patient 19 years or younger at the time of the agreement acquisition

研究者

发起方
Fujita Health University respiratory medicine department

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