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临床试验/NCT00261248
NCT00261248已完成2 期

Phase 2 Clinical Trial of Vaginal Mucosal Immunization for Recurrent Urinary Tract Infections

University of Wisconsin, Madison2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 1996年11月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
75
试验地点
2
主要终点
Rate of re-infection over the study

研究概览

简要总结

The purpose of this study is determine whether a vaginal mucosal vaccine given to women with a history of recurrent urinary tract infections can reduce the number of infections occurring in a six-month study period, as compared to placebo treatment.

详细描述

Recurrent urinary tract infections (UTIs) affect approximately 10% of women in the United States. Since antibiotic prophylaxis is not always effective, alternate treatments need to be developed. One such treatment would be immunization with a vaccine containing bacteria known to cause these infections. The objective of the study is to immunize susceptible women with inactivated bacteria contained in a vaginal suppository and to monitor the rates of reinfection compared to a group of women treated with placebo suppositories. Each group of patients will receive a total of six suppositories in the first four-months of the six-month study during which all UTIs and side effects will be recorded. The infection rates between vaccine- and placebo-treated women will be statistically analyzed to determine vaccine efficacy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Three or more urinary tract infections in the previous year

排除标准

  • Neurogenic bladder
  • Interstitial cystitis
  • Urinary diversion
  • Kidney stones
  • Indwelling catheter

结局指标

主要结局

Rate of re-infection over the study

次要结局

  • Infection-free status at completion of study

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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