NL-OMON48757已完成不适用
Prediction of preeclampsia and adverse events - PREPARE
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 400
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 64（—）
入选标准
- •1) Age * 16 years;2) Gestational age of at least 20 weeks and 0 days;3) Signed written informed consent;4) Suspected preeclampsia as a protocol defined definition , based on one or more of the following criteria:
- •- New onset of elevated blood pressure (BP)
- •- Aggravation of preexisting hypertension
- •- New onset of protein in urine
- •- Aggravation of preexisting proteinuria
- •- One or more other reason(s) for clinical suspicion of PE:
- •* PE-related symptoms: epigastric pain, excessive edema, severe swelling (face, hands, feet), headache, visual disturbances, sudden weight gain (>1 kg/week)
- •* PE-related findings: low platelets, elevated liver transaminases, IUGR (Intra-uterine growth restriction);OR;5) Confirmed preeclampsia as defined by the International Society for the Study of Hypertension in Pregnancy (ISSHP)
排除标准
- •1) Insufficient understanding of Dutch language
研究者
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