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临床试验/CTRI/2018/04/012961
CTRI/2018/04/012961已完成未知

International pregnancy cohort study to evaluate the effect of influenza virus infection on pregnancy and perinatal outcomes and estimate the vaccine-preventable incidence of influenza during pregnancy among women in low- and middle-income countries - PRIME

Abt Associates Inc through CDC Atlanta0 个研究点目标入组 5,000 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
5,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Aged >=18 years;
  • Pregnant as confirmed by urine pregnancy test and/or abdominal ultrasound;
  • Have an estimated date of delivery (EDD) based on LMP or ultrasound
  • othat occurs at least 8 weeks after the anticipated start date of the influenza season for women enrolled prior to that date;
  • othat occurs at least 8 weeks after enrollment for women enrolled after the anticipated start date of the influenza season;
  • Meet one of the following criteria:
  • ohave had an ultrasound at <28 weeks gestation to establish her EDD at a facility where medical records are available for verification of ultrasound results;
  • ocurrently at <28 weeks gestation based on her reported EDD or LMP and willing to undergo a trans-abdominal ultrasound for pregnancy dating as part of the study;
  • Plan to remain in the study area for the duration of her pregnancy and for her delivery;
  • Be willing and able to be contacted twice weekly by telephone call, mobile phone text message, or home visit from enrollment through the end of pregnancy;

排除标准

  • Aged <18 years;
  • Plans for delivery outside the study area;
  • Unable to give consent;

研究者

发起方
Abt Associates Inc through CDC Atlanta

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