跳至主要内容
临床试验/KCT0004837
KCT0004837尚未招募未知

Evaluation of the Effectiveness of Terazosin in Patients with Nocturia due to Prostate Hyperplasia

Hanyang University Guri Hospital0 个研究点目标入组 82 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
82

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
19(Year) 至 o Limit(—)
性别
Male

入选标准

  • 1. An adult male over 19 years of age
  • 2. Persons with an IPSS total score of 8 or higher
  • 3. Persons with a maximum urinary speed (Qmax) of less than 15mL/s
  • 4. Persons with a single urinary volume of 150 mL or higher
  • 5. Persons with more than one night urination
  • 6. Those who have agreed to participate in this research under the signature of their own handwriting

排除标准

  • 1. Those who are overreacting to Alpha-Blocker drugs
  • 2. Person with bladder neck stenosis and urinary tract stenosis
  • 3. Persons with renal dysfunction (Creatine concentration in the serum >2.0 mg/dL)
  • 4. A person with severe liver failure or with a history of illness.
  • 5. Those with severe cardiovascular disease
  • 6. A person with severe low blood pressure
  • 7. Other persons who are not qualified to participate in this study as the Director of Research judges

研究者

相似试验

Evaluation of the Effectiveness of Terazosin in... | 临床试验