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临床试验/NCT02911662
NCT02911662终止不适用

Treatment of Asymptomatic Bacteriuria in Pregnancy

Saint Joseph Mercy Health System1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2016年9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
状态
终止
入组人数
13
试验地点
1
主要终点
Evidence that 3-day treatment is as effective as 7-day treatment of asymptomatic bacteriuria in pregnancy.

研究概览

简要总结

This is a prospective randomized controlled day comparing the efficacy of three-day antimicrobial treatment of asymptomatic bacteriuria (ASB) in pregnancy to the standard seven-day treatment. Half the patients will receive 3-day treatment and the other half will receive 7 days of antibiotics.

详细描述

The current standard of practice is to treat pregnant patients with ASB with a 7-day course of oral antimicrobial agents. If bacteriuria persists women are retreated with the same of different agent for a second course of 7 to 14 days and they may be subsequently placed on prophylaxis.

In nonpregnant women, an uncomplicated lower urinary tract infection may be treated with a short course regimen from 1 to 3 days. This approach has similar rates of persistent bacteriuria or symptoms following treatment when compared to women treated with a more conventional approach. If the infection recurs or persists, the patient may then be treated with the more traditional 7 to 14 day course. The advantages of single-dose regimens are cost and patient compliance, but a major disadvantage is the failure to eradicate uropathogens from the vaginal reservoir, which results in more frequent early recurrences.

The three-day regimen is advocated to maintain the advantages of lower costs and patient compliance but improving cure rates. Multiple studies have shown the advantage of even a short course of antibiotics as opposed to no treatment.

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
None

入排标准

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

入选标准

  • Pregnant women ≥ 18 years of age seeking prenatal care at the Academic Obstetrics and Gynecology Center at St. Joseph Mercy Hospital, Ann Arbor, Michigan
  • Randomization will occur if the patient every has a urine culture demonstrating ≥10,000 cfu/ml of a pathogenic urinary tract organism

排除标准

  • Symptomatic bacteriuria (cystitis or pyelonephritis) at the time of urine collection
  • Previously treated bacteriuria in current pregnancy
  • Past medical history of known congenital or acquired urinary tract anomaly or abnormality (i.e. pelvic kidney, single kidney, renal transplant)
  • Any antibiotic use within the week prior to urine sampling
  • Urine culture revealing growth of the following organisms: Lactobacillus, coagulase-negative staphylococcus

研究组 & 干预措施

3-day treatment

Experimental

Three-day treatment with Cephalexin or Nitrofurantoin for diagnosis of asymptomatic bacteriuria in pregnancy.

干预措施: Cephalexin (Drug)

3-day treatment

Experimental

Three-day treatment with Cephalexin or Nitrofurantoin for diagnosis of asymptomatic bacteriuria in pregnancy.

干预措施: Nitrofurantoin (Drug)

7-day treatment

Active Comparator

Seven-day treatment with Cephalexin or Nitrofurantoin for diagnosis of asymptomatic bacteriuria in pregnancy.

干预措施: Cephalexin (Drug)

7-day treatment

Active Comparator

Seven-day treatment with Cephalexin or Nitrofurantoin for diagnosis of asymptomatic bacteriuria in pregnancy.

干预措施: Nitrofurantoin (Drug)

结局指标

主要结局

Evidence that 3-day treatment is as effective as 7-day treatment of asymptomatic bacteriuria in pregnancy.

时间窗: Within 21 days of treatment

Comparison of percentage of women in each group with successful treatment or asymptomatic bacteriuria with negative urine culture 2 weeks after randomized treatment.

次要结局

  • Comparison of development of cystitis during pregnancy.(Until 6 weeks postpartum)
  • The occurence of preterm delivery(Assessed at the time of delivery)
  • Comparison of development of pyelonephritis during pregnancy(Until 6 weeks postpartum)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Pooja Green

Director of Obstetrical Research

Saint Joseph Mercy Health System

研究点 (1)

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