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临床试验/JPRN-jRCT2080220026
JPRN-jRCT2080220026未知3 期

CS-801 phase 3 long-term study

Sankyo Co.,Ltd.0 个研究点开始时间: 2005年9月5日最近更新:
适应症

试验速览

阶段
3 期

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
>= 20age old 至 ot applicable(—)

入选标准

  • -Patient, age 20 years or older
  • -Patients with urinary frequency and urge urinary incontinence
  • Exclusion criteria:
  • -Patients who have diseases such as dysuria or urinary retention
  • -Patients who have difficulty to void for myself
  • -Patients with other diseases which may have been related to the state of urination. (ex urinary tract infection)
  • -Patients with polyuria
  • -Patients with diseases for which treatment with anticholinergic agents is contraindicated
  • -Patients in whom precautions are required for the use of anticholinergic agents
  • -Patients who have difficulty to use transdermal medications

排除标准

  • 未提供

研究者

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CS-801 phase 3 long-term study | 临床试验