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临床试验/KCT0004566
KCT0004566尚未招募未知

In patients with benign prostate hyperplasia who received tamsulosin 0.2 mg for more than 4 weeks, the improvement of the lower urinary tract symptom terazosin 5 mg administered for 12 weeks

Dankook Univeristy Hospital0 个研究点目标入组 51 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
51

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
40(Year) 至 o Limit(—)
性别
Male

入选标准

  • 1) Male over 40 years
  • 2) Patients diagnosed with benign prostatic hyperplasia
  • 3) Patients have an IPSS score of at least 8
  • 4) Patients who have been prescribed Tamsulosin 0.2mg for more than 4 weeks but have no significant improvement in IPSS score or maximum urinary velocity (Qmax)
  • 5) Patients who voluntarily decided to participate in this study and agreed in writing to the subject consent form

排除标准

  • 1) Patients with hypersensitivity to a-blocker family drugs.
  • 2) Patients who are taking cholinergic drugs, diuretics, or ß3-antagonists.
  • 3) Patients with urination disorders due to obvious causes other than benign prostatic hyperplasia.
  • 4) Patients with neurogenic bladder disorders.
  • 5) Patients with urinary tract infections (midstream urine culture> 100,000 colonies/mL)
  • 6) Patients with clinically significant circulatory disorders (myocardial infarction, heart failure, angina pectoris, cardiac arrhythmias, pacemaker use, orthostatic hypotension, uncontrolled hypotension)
  • 7) Participants in other interventions within 6 months of screening
  • 8) Patients who are inappropriate to participate in research as judged by other research managers or researchers

研究者

发起方
Dankook Univeristy Hospital

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