跳至主要内容
临床试验/KCT0005736
KCT0005736尚未招募未知

A comparative study on the treatment effect of Hytrin alone or Hytrin/Hinechol combined administration to patients with prostatic hyperplasia with lower urinary tract symptoms (LUTS)

Cheongju ST.Mary's Hospital0 个研究点目标入组 200 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
200

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) Men over 40 years old
  • 2) Those with a total score of 8 or more in the International Prostate Symptom Score (IPSS)
  • 3) Those who voluntarily decide to participate in this study and consent in writing to the subject's consent

排除标准

  • 1) Those with hypersensitivity to Hythrin-based drugs (alpha-blocker) and Heinecol-based drugs (cholinergic drugs)
  • 2) Those with clinically significant circulatory diseases (myocardial infarction, heart failure, angina, deep veins, pacemaker use, orthostatic hypotension, uncontrolled hypotension)
  • 3) Those on hemodialysis
  • 4) Those who show persistent oliguria due to renal function abnormalities
  • 5) Patients with moderate hepatic impairment (Child-Pugh grade B)
  • 6) Those who participated in other interventional clinical trials within 6 months of screening
  • 7) Those who have a history of or present malignant tumors, and who are inadequate to participate in the study as judged by the principal investigator or the investigator.
  • 8) Asthma patients, patients with hyperthyroidism
  • 9) Others who are inadequate to participate in the research as judged by theprincipal investigator or the investigator.

研究者

发起方
Cheongju ST.Mary's Hospital

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