跳至主要内容
临床试验/jRCT2080220025
jRCT2080220025未知3 期

CS-801 phase 3 comparative study

Sankyo Co.,Ltd.0 个研究点开始时间: 待定

试验速览

阶段
3 期
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
干预模型
Double blind comparative study

入排标准

年龄范围
20age old over 至 No limit(—)

入选标准

  • Inclusion criteria:
  • 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

结局指标

主要结局

-

Efficacy and safety

次要结局

未报告次要终点

研究者

相似试验

CS-801 phase 3 comparative study | 临床试验