ISRCTN44316210已完成未知
The safety of outpatient compared to inpatient treatment in women with PPROM prior to 34 weeks of gestation: a randomized controlled trial
Helsinki University Hospital0 个研究点目标入组 126 人开始时间: 2018年5月11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
- 126
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. PPROM at gestational weeks 20+0 to 33+6
- •2. No clinical signs of infection
- •3. No subclinical infection in amniocentesis
- •4. Willing to participate
- •5. Singleton pregnancy
排除标准
- •1. Severe Intrauterine growth restriction (IUGR) or redistribution in fetal blood flow
- •2. Symptomatic pre-eclampsia, or pre-eclampsia with blood pressure medication, proteinuria, or abnormal laboratory values
- •3. Clinical infection in vagina or uterus, or HIV infection
- •4. Inadequate language skills to understand the written medical consent or handout of the study
- •5. Diabetes Type 1
研究者
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