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临床试验/NCT00913315
NCT00913315Unknown不适用

Efficacy Study of Tamsulosin and Tolterodine Treatment of Men With Chronic Prostatitis/Chronic Pelvic Pain Syndrome and Lower Urinary Tract Symptoms

Chongqing Medical University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2009年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
30
试验地点
1
主要终点
National Institutes of Health Chronic Prostatitis Symptom Index

研究概览

简要总结

The purpose of this study is to determine whether tamsulosin and tolterodine are effective in the treatment of men with lower urinary tract symptoms and chronic prostatitis/chronic pelvic pain syndrome.

详细描述

Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) is a common disorder in urological clinics. Most of the clinically CP/CPPS are to some extent associated with storage (irritative) symptoms, such as increased frequency, urgency, and nocturia, namely many patients with CP/CPPS have overactive bladder symptoms. Alpha-blocker therapy has been advocated as a treatment modality for CP/CPPS. Some trials showed a statistically and likely clinically significant treatment effect, while other trials showed no benefit. Therefore, tamsulosin combination with tolterodine treatment for CP/CPPS may be more effective than tamsulosin single.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • diagnosis of CP/CPPS based on the classification of US National Institutes of Health, aged 18-45 years
  • total score of at least 12 on the National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI)
  • urinary score of at least 4 on the CPSI
  • subjects who anticipate improving symptoms

排除标准

  • previous treatment with any other alpha-adrenergic receptor blocker and antimuscarinic agents for symptoms of CP/CPPS or for any other reason
  • those who had had previous urinary tract infection with the last year
  • those who had been treat or were taking medication that could affect lower urinary tract function
  • those who met the criteria for chronic bacterial prostatitis after lower urinary tract localization studies
  • those who had other significant medical problems

研究组 & 干预措施

tolterodine + tamsulosin

Experimental

干预措施: tolterodine (Drug)

tolterodine + tamsulosin

Experimental

干预措施: tamsulosin (Drug)

tamsulosin + placebo

Active Comparator

干预措施: tamsulosin (Drug)

tamsulosin + placebo

Active Comparator

干预措施: placebo (Drug)

结局指标

主要结局

National Institutes of Health Chronic Prostatitis Symptom Index

时间窗: 4 months

次要结局

  • International Index of Erectile Function(4 months)
  • Peak urinary flow rate(4 months)

研究者

发起方
Chongqing Medical University
申办方类型
Other

研究点 (1)

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