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临床试验/CTRI/2021/03/031758
CTRI/2021/03/031758已完成未知

To evaluate docosahexaenoic acid baseline reference ranges in Indian pregnant population and establishing the preclinical data in the treatment of preterm birth. - DCNPW

Department of Pharmaceutical Sciences Guru Nanak Dev University Amritsar0 个研究点目标入组 164 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
164

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

入选标准

  • Women were eligible for enrollment if they were between 12 and 24 week of gestation between 16 and 40 year of age and planning to deliver at a same hospital

排除标准

  • You have an active infection or other serious condition such as cardiac disease, cancer, lupus, hepatitis, HIV/AIDS, or a diagnosed alcohol or chemical dependency.
  • Subjects were excluded if they were carrying more than one fetus.
  • Had preexisting diabetes mellitus or systolic blood pressure 140 mm Hg at enrollment.
  • Had any serious health condition likely to affect the prenatal or postnatal growth and development of their offspring,
  • You are unable or unwilling to DHA supplement.
  • You have had a yellow fever vaccination within the last 30 days or plan to have it.

研究者

发起方
Department of Pharmaceutical Sciences Guru Nanak Dev University Amritsar

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