跳至主要内容
临床试验/IRCT201507313944N4
IRCT201507313944N4已完成4 期

Comparison of high dose and low dose folic acid supplementation on prevalence, onset and severity of preeclampsia

Isfahan University of Medical Sciences0 个研究点目标入组 900 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
900

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

年龄范围
17 years 至 40 years(—)
性别
Female

入选标准

  • all of women with living fetus in the uterine cavity in first trimester with willingness for participation in this study, were included and do not: Presence or history of a disorder in which administration of folic acid is contraindicated, renal diseases, using anti-epileptic drugs (since the metabolism of anti-epileptic drugs requires a great deal of folic acid), malignancy, alcohol abuse, multiple birth (presence of three living fetus or more) and known hypersensitivity to folic acid (rashes, dermatologic and gastroenterological discomforts).
  • Exclusion criteria: Fetal death during the study, major abnormality of the fetus, women who were planning to move outside of the catchment area of the study within the pregnancy duration.

排除标准

  • 未提供

研究者

相似试验

High dose folic acid supplementation effect on... | 临床试验