JPRN-UMIN000002188尚未招募未知
Comparative study of efficacy and safety of Administering 4mg once daily and 2mg twice daily of silodosin in patients with benign prostatic hyperplasia - Comparative study of mode of administration of silodosin
JR Tokyo General Hospital0 个研究点目标入组 100 人开始时间: 2009年8月1日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 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
- Interventional
入排标准
- 年龄范围
- ot applicable 至 ot applicable（—）
- 性别
- Male
入选标准
- 未提供
排除标准
- •1.Men who treated by the medicin that has possibility to influence the urination function 2.prostatic cancer 3.Urinary tract infection 4.urolithiasis 5.hepatic dysfunction, renal dysfunction, cardiac disease 6.orthostatic hypotention 7.Any other clinically relevant laboratory abnormality as judged by the investigator
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