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临床试验/PACTR202401619811584
PACTR202401619811584尚未招募4 期

Weekly doxycycline DOT for STI prevention among cisgender women taking HIV PrEP in Kisumu, Kenya

niversity of Washington0 个研究点目标入组 60 人开始时间: 2024年1月18日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
60

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
13 Year(s) 至 18 Year(s)(—)
性别
Female

入选标准

  • 1)Willing and able to give written informed consent
  • 2)Age 18-30 years
  • 3)Female sex at birth
  • 4)HIV-seronegative, according to national HIV testing algorithm
  • 5)Has a current prescription for PrEP, according to the national guidelines of Kenya
  • 6)Able and willing to adhere to DOT dosing schedules

排除标准

  • 1)Pregnant
  • 2)Breastfeeding a child
  • 3)Allergy to tetracycline class
  • 4)Current medications which may impact doxycycline metabolism or that are contraindicated with doxycycline, as per the prescribing information. These include systemic retinoids, barbiturates, carbamazepine, phenytoin, and warfarin.
  • 5)Active, clinically significant medical or psychiatric conditions that would interfere with study participation, at the discretion of the site investigator or designee.
  • 6)Prior enrollment in The dPEP Kenya Study

研究者

发起方
niversity of Washington

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