ISRCTN11966080已完成未知
A multicentre, double blind, placebo controlled, randomised trial to evaluate the effectiveness of a 1-day versus 7-day regimen of nitrofurantoin for the treatment of asymptomatic bacteriuria in pregnancy
World Health Organization (WHO) (Switzerland)0 个研究点目标入组 778 人开始时间: 2007年12月14日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 778
研究概览
简要总结
2009 results in https://pubmed.ncbi.nlm.nih.gov/19155904/ (added 30/12/2020)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Pregnant women with gestational age 12 - 32 weeks
- •2. Willing and able to give consent
排除标准
- •1. Have any underlying disease, which require continuous steroid and/or antibiotic treatment, e.g. systemic lupus erythematosus, valvular heart disease, etc.
- •2. Use of any antibiotics during the past one-week
- •3. Received any treatment for urinary tract infection at any time during the current pregnancy
- •4. History of nitrofurantoin hypersensitivity
- •5. Plan not to deliver at the study hospital
- •6. Any symptoms such as flank pain, dysuria that suggests symptomatic Urinary Tract Infections (UTI)
- •7. Have any haematological disease including Glucose-6-Phosphate Dehydrogenase deficiency (G6PD)
- •8. Negative urine dipslide
- •9. Negative urine culture
- •10. Positive urine culture but the organism is resistant to Nitrofurantoin
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