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临床试验/NCT03852849
NCT03852849Unknown不适用

Cohort Study on Appropriate Strategies of The Rapid Build of HIV Related Protective Barriers in Yunnan, China

National Center for AIDS/STD Control and Prevention, China CDC2 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2019年3月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
600
试验地点
2
主要终点
Viral suppression of HIV-infected patients

研究概览

简要总结

The purpose of the study is to screen the optimal intervention strategies to rapid establish the protective barriers against HIV-infection by maximally decreasing the viremia among HIV- infected patients.

详细描述

Sexual transmission became the primary route of HIV transmission in China and heterosexual transmission also contributed greatly to HIV epidemic which was mostly reported in South-west rural areas. In past years, Yunnan has experienced powerful campaign of scaling-up the HIV identification as well as antrertroviral therapy.

This study will investigate how to reach the last two of HIV'90-90-90 targets': to provide antiretroviral therapy (ART) for 90% of who diagnosed HIV infection and to achieve viral suppression for 90% of those treated.

The study population consists of participants who received an newly diagnosed HIV infection within the study period. All rerolled participants will be randomized into different study group. In intervention group, medical institutions will provide patients personal involved intervention strategies which guided by frequent viral load detection, and providing of the dosage form of 400 mg EFV in their antiviral therapy.

Main assessment measures are viral suppression rate of HIV-infected patients and treatment coverage .

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • HIV-positive participants who received an newly diagnosed HIV infection within the study period
  • Having a current residential address inside of pilot site limits
  • Eighteen years old or above
  • HIV transmission is heterosexual contact

排除标准

  • Having severe mental disorder

研究组 & 干预措施

medicine intervention group

Experimental

The dosage of 400 mg EFV will be used in the antiviral therapy.

干预措施: The dosage of 400mg EFV (Drug)

consolidated intervention group

Experimental

Medical institutions will provide personal involved intervention strategies as well as the providing of dosage form of 400 mgEFV in their antiviral therapy.

干预措施: Personal involved intervention strategies (Behavioral)

consolidated intervention group

Experimental

Medical institutions will provide personal involved intervention strategies as well as the providing of dosage form of 400 mgEFV in their antiviral therapy.

干预措施: The dosage of 400mg EFV (Drug)

结局指标

主要结局

Viral suppression of HIV-infected patients

时间窗: 12 months

次要结局

  • Treatment coverage(12 months)

研究者

发起方
National Center for AIDS/STD Control and Prevention, China CDC
申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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