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临床试验/JPRN-jRCT2080225317
JPRN-jRCT2080225317已完成2 期

A Randomized, Double-blind, Cross-over Study of S-600918 in Participants with Sleep Apnea Syndrome

SHIONOGI & CO., LTD.0 个研究点目标入组 33 人开始时间: 2020年8月18日最近更新:
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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