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临床试验/NCT03827278
NCT03827278Unknown不适用

Human Immunodeficiency Virus Negative Host Talaromyces Between Voriconazole and Amphotericin B Sequential Itraconazole Therapy

Guangxi Medical University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年12月30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
200
试验地点
1
主要终点
Number of Participants with all-cause mortality

研究概览

简要总结

Through a multi-center large-sample non-randomized controlled study, the effect of voriconazole, amphotericin B sequential itraconazole therapy on Talaromyces in Human Immunodeficiency Virus(HIV)negative hosts were compared to clarify whether the two therapies were equivalent; A comprehensive efficacy evaluation system and standard treatment program was established to provide a basis for standardized treatment of Talaromyces in Human Immunodeficiency Virus negative hosts.The observational indicators included: 2-week all-cause mortality; 24-week all-cause mortality; clinical improvement time; level of decrease of fungus in the blood culture medium two weeks before treatment; recurrence; appearance of adverse drug reaction at the level 3 and above. Dynamically monitor the immune cells and factors like anti-Interferon-γ autoantibodies, Interferon-γ, Th1/Th2, and Th17/Treg in the HIV-negative Talaromyces host microenvironment, and observe the host's immune status and its change. 3. study the effect of absence of Interferon-γ and Interferon-γ Receptor (IFN-γR)on the activation and function of anti-Interferon-γ autoantibodies, Th1/Th2, and Th17/Treg by establishing a Talaromyces mouse model that knocks out the Interferon-γ and IFN-γR gene and a IFN-γ silenced cell model; Study the effect of anti-IFN-γ autoantibody on the activation and function of IFN-γ、Th1/Th2、Th17/Treg by increasing its titer in vitro and vivo; determine by which path the anti-IFN-γ autoantibody of HIV-negative host influences its immune regulation mechanism; finally, the intervention effect of IFN-γ on high titer anti-IFN-γ autoantibodies is studied, providing a new idea for immunotargeted therapy.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • HIV-negative adults (≥18 years of age) who diagnosis of talaromyces that was confirmed by either microscopy or culture
  • Must be able to swallow tablets

排除标准

  • Pregnancy, central nervous system involvement assessed either clinically or by analyses of cerebrospinal fluid
  • An allergy to voriconazole, itraconazole or amphotericin
  • The concomitant use of certain medications that interact with voriconazole, itraconazole or amphotericin
  • An alanine aminotransferase or aspartate aminotransferase level of more than 400 U per liter
  • An absolute neutrophil count of less than 500 per cubic millimeter
  • A creatinine clearance of less than 30 ml per minute (calculated by the method of Cockcroft and Gault)
  • a concurrent diagnosis of cryptococcal meningitis
  • concurrent treatment with rifampicin
  • previous treatment for talaromyces for more than 48 hours
  • HIV positive who diagnosis of talaromyces.

研究组 & 干预措施

HIV Negative Host talaromyces using Voriconazole

Experimental

Voriconazole On the first day, 6 mg/kg bid was given, and then 4 mg/kg bid was given intravenously for 6 days, and then oral voriconazole 200 mg bid was administered to maintain treatment for at least 6 months.

干预措施: Voriconazole (Drug)

HIV Negative talaromyces AMB Sequential Itraconazole

Experimental

Amphotericin B (AMB) sequential itraconazole group (intravenous amphotericin, dose 0.7 - 1.0 mg / kg / d, 14 days, then changed oral itraconazole 200 mg bid for 10 weeks, after which 100 mg bid maintenance Until cluster of differentiation 4 (CD4+ T) cells are greater than 100 cells/L for at least 6 months

干预措施: Voriconazole (Drug)

结局指标

主要结局

Number of Participants with all-cause mortality

时间窗: up to 24 weeks

defined as the absolute risk of death from any cause during 24 weeks

Number of Participants with Clinical resolution of talaromyces

时间窗: 3 days

Clinical resolution of talaromyces was defined as a temperature of less than 38°C (100°F) for 3 days, resolution of skin lesions, and tertile blood cultures. Early fungicidal activity was defined as the rate of decline in blood T. marneffei colony forming units (CFUs).

Number of Participants with Early fungicidal activity

时间窗: up to 2 weeks

defined as the rate of decline in blood T. marneffei CFUs from sterical blood cultures obtained during the first 2 weeks.

Number of Participants with Relapse of talaromyces

时间窗: an average of 1 year

defined as the recurrence of symptoms and a positive fungal culture from any sterile site that led to reinduction of therapy in patients who had achieved clinical resolution.

次要结局

未报告次要终点

研究者

发起方
Guangxi Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Qiu Ye

Clinical Professor

Guangxi Medical University

研究点 (1)

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