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临床试验/NCT00210886
NCT00210886已完成3 期

A Multicenter, Double-blind, Randomized Study to Compare the Efficacy and Safety of Levofloxacin 750 mg Once Daily for Five Days Versus Ciprofloxacin Twice Daily for Ten Days in the Treatment of Complicated Urinary Tract Infection and Acute Pyelonephritis.

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.0 个研究点目标入组 1,109 人开始时间: 2004年10月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
1,109
主要终点
Combination of clinical success and microbiologic eradication (known as therapeutic response) at post-therapy visit.

研究概览

简要总结

The purpose of this study is to evaluate the effectiveness and safety of two antibiotics in the treatment of complicated urinary tract infection or acute pyelonephritis (kidney infection). A 5-day course of 750 milligrams of levofloxacin given intravenously and/or by mouth once daily will be compared to a 10-day course of 400 milligrams of ciprofloxacin given intravenously and/or 500 milligrams of ciprofloxacin given by mouth twice daily.

详细描述

Levofloxacin has been approved in both its oral and intravenous forms to treat a large number of infections caused by bacteria. Levofloxacin and other members of a class of antibiotics known as fluoroquinolones have been used successfully to treat urinary and kidney infections. This study will compare the effectiveness and safety of levofloxacin given for 5 days to that of another fluoroquinolone, ciprofloxacin, given for 10 days in treating complicated urinary tract infection or acute pyelonephritis (kidney infection). A shorter course of antibiotics may help patients take all of their medication, which is critically important for curing the infection. A shorter course may also help prevent the development of bacteria that cannot be killed by antibiotics. Patients will take 750 milligrams of levofloxacin intravenously and/or by mouth once daily for 5 days or 400 milligrams of ciprofloxacin intravenously and/or 500 milligrams of ciprofloxacin by mouth twice daily for 10 days. To prevent the study doctor, study staff and patients from knowing which study drug they are taking, all study drug will manufactured to look the same and patients on the 5-day regimen will be given placebo for the last 5 days of their participation in the study. The intravenous infusion bags will be covered so that the solution cannot be seen. The objective of the study is to demonstrate that 5 days of levofloxacin once daily is at least as effective as 10 days of ciprofloxacin twice daily in treating complicated urinary tract infection or acute pyelonephritis. Patients will take 750 milligrams of levofloxacin intravenously and/or by mouth once daily for 5 days or 400 milligrams of ciprofloxacin intravenously and/or 500 milligrams of ciprofloxacin by mouth twice daily for 10 days.

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

入排标准

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

入选标准

  • Positive dipstick test for leukocyte esterase AND/OR at least 5 white blood cells per centrifuged urine sediment AND/OR at least 10 white blood cells per microliter of uncentrifuged urine
  • outpatient or inpatient (in hospital, nursing home, or other extended-care facility)
  • clinical diagnosis of either complicated urinary tract infection or acute pyelonephritis.

排除标准

  • Allergy or serious adverse reaction to levofloxacin, ciprofloxacin, or other fluoroquinolone
  • urinary tract surgery or lithotripsy (treatment for kidney stones) within 7 days before study entry
  • a second coexisting bacterial infection that requires systemic antibiotics
  • need for a second antibiotic to treat the urinary tract infection
  • obstruction of the urinary tract
  • prostate infection.

结局指标

主要结局

Combination of clinical success and microbiologic eradication (known as therapeutic response) at post-therapy visit.

次要结局

  • By patient and pathogen microbiologic and clinical responses at the post-therapy and post-study visits.

研究者

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