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临床试验/KCT0000091
KCT0000091已完成未知

Clinical Study of Efficacy and Safety of Baweidihuang-wan in patients with Overactive Bladder

Dongguk University0 个研究点目标入组 186 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
186

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
Female

入选标准

  • 1) female aged more than 40
  • 2) symptoms of urinary urgency and frequency more than 3months.
  • 3) korea OABSS >3 at first visit
  • 4) after first visit, URS=2 and urination number per day >8 and/or urge incontinence
  • 5) agreed the study

排除标准

  • 1) diagnosed UTI in U/A
  • 2) stress incontinence without symptoms of OAB
  • 3) suspicious neurologic bladder
  • 4) history of cystocele, hysterocele
  • 5) history of obstrcutive uropathy ; urolithiasis, tumor, etc
  • 6) history of bladder surgery
  • 7) history of urinary malignant tumor
  • 8) history of neuropsychiatric disease (schizophrenia, drug addiction, epilepsy, etc)
  • 9) The other condition, which makes the patient unsuitable for inclusion in the opinion of investigator
  • (uncontrolled HTN, DM, thyroid disease, acute, chronic hepatitis/cirrhosis, severe hyperlipidemia, severe heart disease, Tbc, ather infectional disease)
  • 10) hypersensitivity, allergy og the study related drug
  • 11) OMD diagnose '????' ; dehydration oral cavitiy, redness of tongue, face, eyes, sweating at night, etc
  • 12) parcipication in other clinical trial within 3months
  • 13) use of drugs within 1months preceding bladder function
  • (Tolterodine, Trospium, Solifenacin, Propantheline, Atropine, Hyoscyamine, Fesoterodine fumarate, Oxybutynin, Propiverine, Imipramine, Alfuzosin, Doxazocin, Prazosin,Terazosin, Tamsulosin, etc)
  • 14) unsuitable condition which intake herb medication because of systemic disease
  • 15) person who did not writing

研究者

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