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临床试验/CTRI/2013/04/003540
CTRI/2013/04/003540已完成3 期

Effect of Docosa-hexaenoic acid (DHA) Supplementation during pregnancy on Newborn outcomes in India â?? the DHANI randomized controlled trial - DHANI- RCT

Department of Science and Technology0 个研究点目标入组 957 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
957

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

  • a) 18-35 y old pregnant women (singleton) at <20 weeks of gestation (calculated from the last menstrual period or by ultrasound in 1st trimester as suggested by study physician/team).
  • b) Willing to participate in the study and provide all measurements for her and the offspring including anthropometry, dietary assessment and questionnaires plus the biochemical parameters (blood, breast milk)
  • c) Witnessed informed consent signed by mother.
  • d) Plans to deliver at the study hospital (under JNMC, Belgaum)

排除标准

  • a) Women allergic (if aware) to any of the test products.
  • b) Women with any known history of bleeding tendency or thrombosis (if aware).
  • c) Women with high-risk pregnancies â??
  • - any bleeding episode in the current pregnancy;
  • - hypertension;
  • - diagnosed heart disease;
  • - diabetes
  • d) Women consuming omega-3 supplements or having used these in 3 months preceding the intervention period.
  • e) Reported participation in another biomedical trial 3 months before the start of the study or during the study (not to get the results of the present study contaminated).

研究者

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