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临床试验/ISRCTN62368611
ISRCTN62368611已完成未知

A randomised controlled trial of vitamin C and E supplementation to prevent pre-eclampsia in women at risk

King's College London (UK)0 个研究点目标入组 2,400 人开始时间: 2003年11月17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
2,400

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

  • Women with identified additional risk factors for pre-eclampsia in ten geographical areas, and 22 hospitals through England:
  • 1. Pregnant women between 14 and 22 weeks' gestation
  • 2. A history of pre-eclampsia (requiring delivery less than 37 weeks) in preceding pregnancy, eclampsia or Haemolysis, Elevated Liver enzyme levels and Low Platelet count (HELLP) syndrome (at any time)
  • 3. Women with essential hypertension, diabetes (requiring treatment), Systemic Lupus Erythrematosus (SLE)/Anti-Phospholipid antibody Syndrome (APS) with renal imvolvement
  • 4. In the current pregnancy: abnormal uterine artery Dopplers (18 to 22 weeks), multiple pregnancy, diastolic Blood Pressure (BP) more than 90 mmHg (before 20 weeks)
  • 5. Primparous women with Body Mass Index (BMI) more than 30

排除标准

  • 1. Inability/unwillingness to give informed consent
  • 2. Women taking warfarin (due to the theoretical potentiation of warfarin by Vitamin E)

研究者

发起方
King's College London (UK)

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