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临床试验/IRCT201008112624N7
IRCT201008112624N7已完成3 期

Evaluating the effect of copper supplement during pregnancy on premature and pregnancy outcome

Deputy of Research and Technology, Iran University of Medical Sciences0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
200

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
18 years 至 35 years(—)
性别
Female

入选标准

  • nuliparity, age between 18-35, second trimester of pregnancy, and having written consent. Exclusion criteria: multiple pregnancy, history of any systemic disorders or drug use except iron supplement, known copper sensitivity, polyhydramnios, fetal death, fetal anomalies, smoking, alcohol consumption and drug abuse.

排除标准

  • 未提供

研究者

发起方
Deputy of Research and Technology, Iran University of Medical Sciences

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Copper prescription in pregnancy | 临床试验