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Effect of Folic Acid Supplementation in Pregnancy on Preeclampsia: The Folic Acid Clinical Trial Study

机译:妊娠期补充叶酸对子痫前期的影响:叶酸临床试验研究

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摘要

Preeclampsia (PE) is hypertension with proteinuria that develops during pregnancy and affects at least 5% of pregnancies. The Effect of Folic Acid Supplementation in Pregnancy on Preeclampsia: the Folic Acid Clinical Trial (FACT) aims to recruit 3,656 high risk women to evaluate a new prevention strategy for PE: supplementation of folic acid throughout pregnancy. Pregnant women with increased risk of developing PE presenting to a trial participating center between 80/7 and 166/7 weeks of gestation are randomized in a 1 : 1 ratio to folic acid 4.0 mg or placebo after written consent is obtained. Intent-to-treat population will be analyzed. The FACT study was funded by the Canadian Institutes of Health Research in 2009, and regulatory approval from Health Canada was obtained in 2010. A web-based randomization system and electronic data collection system provide the platform for participating centers to randomize their eligible participants and enter data in real time. To date we have twenty participating Canadian centers, of which eighteen are actively recruiting, and seven participating Australian centers, of which two are actively recruiting. Recruitment in Argentina, UK, Netherlands, Brazil, West Indies, and United States is expected to begin by the second or third quarter of 2013. This trial is registered with .
机译:子痫前期(PE)是具有蛋白尿的高血压,其在妊娠期发展并影响至少5%的怀孕。怀孕期间补充叶酸对子痫前期的影响:叶酸临床试验(FACT)旨在招募3656名高危女性,以评估PE的新预防策略:整个怀孕期间补充叶酸。出现在妊娠8 0/7 和16 6/7 周之间的试验参与中心的罹患PE的风险增加的孕妇以1:1的比例随机分配至获得书面同意后,叶酸4.0mg或安慰剂。将分析意向性治疗人群。 FACT研究由加拿大卫生研究院于2009年提供资金,并于2010年获得加拿大卫生部的监管批准。基于网络的随机系统和电子数据收集系统为参与中心提供了一个平台,可对符合条件的参与者进行随机选择并进入实时数据。迄今为止,我们有20个参与的加拿大中心,其中18个正在积极招募中,还有7个参与的澳大利亚中心,其中两个正在积极招募中。预计将于2013年第二季度或第三季度开始在阿根廷,英国,荷兰,巴西,西印度群岛和美国的招聘。

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