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临床试验/JPRN-jRCT1080222454
JPRN-jRCT1080222454未知Unknown

Rozerem 8 mg Tablets specified drug-use survey: <Long-term survey on associated with sleep-onset difficulty > - Transitional survey from the preceding drug-use survey

TAKEDA PHARMACEUTICAL COMPANY LTD.0 个研究点目标入组 100 人开始时间: 2014年4月7日最近更新:
适应症

试验速览

阶段
Unknown
发起方
入组人数
100

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
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • Patients with difficulty falling asleep associated with insomnia who have completed a 4-week follow-up in the preceding drug use surveillance and are able to receive continuous administration of Rozerem Tablets

排除标准

  • Patients with contraindications to Rozerem Tablets
  • [1] Patients with previous history of hypersensitivity to ingredients in Rozerem Tablets
  • [2] Patients with severe liver dysfunction
  • [3] Patients taking fluvoxamine maleate

研究者

发起方
TAKEDA PHARMACEUTICAL COMPANY LTD.

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