跳至主要内容
临床试验/JPRN-UMIN000018743
JPRN-UMIN000018743已完成未知

Evaluation of silodosin versus tadalafil in patients with urination disorders associated with benign prostatic hyperplasia - Evaluation of silodosin versus tadalafil in patients with urination disorders associated with benign prostatic hyperplasia

Kissei Pharmaceutical Co.,Ltd.0 个研究点目标入组 180 人开始时间: 2015年8月21日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
180

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
60years-old 至 ot applicable(—)
性别
Male

入选标准

  • 未提供

排除标准

  • 1) Patients have any of the contraindications listed in the package inserts for silodosin or tadalafil. 2) Patients have prostate cancer. 3) Patients have lower urinary tract symptoms possibly due to urinary tract infection or neurogenic bladder. 4) Patients have used silodosin or tadalafil within 12 weeks prior to Week 0.

研究者

相似试验

Evaluation of silodosin versus tadalafil in patients... | 临床试验