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临床试验/NCT01535469
NCT01535469已完成4 期

Operational Research for Cryptococcal Antigen Screening to Improve ART Survival

University of Minnesota2 个研究点 分布在 1 个国家目标入组 3,049 人开始时间: 2012年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
3,049
试验地点
2
主要终点
Retention in care

研究概览

简要总结

This will be a stepped wedge randomized trial design to evaluate the implementation of cryptococcal antigen (CRAG) screening and preemptive anti-fungal therapy of HIV-infected persons entering antiretroviral therapy (ART) outpatient treatment in Uganda. Those who are ART eligible with a CD4≤100 cells/mcL will have a serum/plasma CRAG performed by lateral flow assay. Those who are CRAG-positive and asymptomatic will be treated with high dose fluconazole. After 6 months survival with retention-in-care will be compared between those who are CRAG+ and CRAG negative

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • HIV-1 infection
  • CD4≤100 cells/mcL
  • Cryptococcal antigen (CRAG) positive
  • age >14 years

排除标准

  • Suspected Cryptococcal meningitis
  • Prior known history of cryptococcal meningitis
  • currently receiving HIV antiretroviral therapy
  • Allergy to any azole antifungal medication
  • Persons with known serious hepatic co-morbidities, transaminitis, or clinical jaundice who should not receive fluconazole in the opinion of the study investigator.
  • Current known pregnancy

研究组 & 干预措施

CrAg Screening and Fluconazole

Experimental

Cryptococcal Antigen (CrAg) Screening with preemptive antifungal treatment per World Health Organization (WHO) guidelines. Randomized Stepped Wedge design of phased implementation.

干预措施: Fluconazole (Drug)

结局指标

主要结局

Retention in care

时间窗: 6-month

1. before/after CRAG screening implementation (All persons) 2. CRAG positive persons treated with high-dose fluconazole as compared to 6-month survival of CRAG negative persons who are eligible for antiretroviral therapy.

次要结局

  • Percentage of participants with symptomatic cryptococcal meningitis(baseline)
  • All-cause discontinuation of fluconazole(6-month)
  • Cryptococcal meningitis-free survival time(6-month)
  • Survival Time(6-month)
  • Uptake of CRAG screening and preemptive treatment(baseline)
  • Time from CRAG+ test to receipt of fluconazole therapy(Days from CD4 testing)
  • Risk factors for symptomatic cryptococcal meningitis(baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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