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临床试验/PACTR201909810587438
PACTR201909810587438招募中4 期

Safety and efficacy of Dolutegravir and EFV400 for pregnant and breastfeeding women: a randomized non-inferiority clinical trial

Hawassa University0 个研究点目标入组 1,830 人开始时间: 2019年9月14日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
1,830

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
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • HIV infected pregnant women who are in their 2nd trimester of pregnancy in Ethiopian and Ugandan
  • recruitment sites.
  • - HIV infected pregnant women who are older than 18 years of age
  • - ART naïve HIV infected pregnant women or women who are on first-line ART during 2nd trimester of
  • pregnancy irrespective of the duration on ART and are willing to be switched to the regimen they are
  • assigned to.
  • - Ability to stay in regular follow up during the duration of pregnancy, delivery and during breast feeding; and,
  • - Consenting to exclusively breastfeed, continue participating in the study during breastfeeding, and to allow
  • their infants to participate in the study.
  • - Consenting to use mandatory long-acting contraception for 48 months post-partum for women assigned to
  • the DTG arm.

排除标准

  • - Being on second-line ART during the first trimester of pregnancy
  • - Presence of co-infection (such as TB) and chronic illnesses including diabetes mellitus (DM), hypertension
  • and cardiac diseases, and bad obstetric history including miscarriage or early neonatal death
  • - Not consenting to participate or to be on long-acting contraception for 48 months post-partum if assigned to
  • the DTG arm.

研究者

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