JPRN-jRCT2080225317已完成2 期
A Randomized, Double-blind, Cross-over Study of S-600918 in Participants with Sleep Apnea Syndrome
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 33
研究概览
简要总结
o obvious improvement in the primary endpoint of the change in AHI at Day 7 from baseline was found after administration of S-600918 300 mg compared with placebo, and the difference between the study drugs was not statistically significant. S-600918 was generally safe and well tolerated at a once daily dose of 300 mg for 7 days.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 <= 70age old(—)
- 性别
- All
入选标准
- •Key Inclusion Criteria:
- •- Participants diagnosed with sleep apnea syndrome or suspected sleep apnea based on the International Classification of Sleep Disorders, Third Edition (ICSD-3).
排除标准
- •Key Exclusion Criteria:
- •- Participants with a clinically significant active respiratory disease.
- •- Participants with obvious morphological abnormalities of the upper respiratory tract, micrognathia, or developmental failure of the mandible.
研究者
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