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临床试验/ISRCTN55813586
ISRCTN55813586已完成不适用

Clinical dosage and effectiveness study of ShanStar® Cranberry supplement for prevention and treatment against women's urinary tract infections: a double blind, randomised, placebo-controlled clinical study

ShanStar Biotech, Inc.0 个研究点目标入组 60 人开始时间: 2011年3月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Age between the age of 18-50
  • 2. Female gender
  • 3. Healthy individual with 3 or more episodes of urinary tract infections per year
  • 4. Able to complete the research study

排除标准

  • 1. Terminal diesease or dementia
  • 2. Abstain from any cranberry, health food fruit extracts, anti-oxidants, vitamins, minerals and antibiotics for 2 weeks prior to participation in the study
  • 3. Pregnancy
  • 4. Urine catherisation within previous 2 weeks of study
  • 5. Participants with history of diabetes, cardiovascular disease, symptoms of pyelonephritis and stones in the urinary tract
  • 6. Sexually transmitted disease
  • 7. Pyuria or bacteriuria on urinalysis or positive urine culture ( will be treated and wait 2 weeks to be eligible)

研究者

发起方
ShanStar Biotech, Inc.

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