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临床试验/NCT00002122
NCT00002122已完成3 期

A Randomized Study of Daily and Intermittent Prophylactic Regimens for the Prevention of Disseminated Mycobacterium Avium Complex (MAC) and Fungal Infections in HIV-Infected Patients

Pfizer12 个研究点 分布在 1 个国家目标入组 720 人开始时间: 2001年8月31日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Pfizer
入组人数
720
试验地点
12

研究概览

简要总结

PRIMARY: To determine the efficacy of azithromycin and rifabutin alone and in combination for the prevention of disseminated Mycobacterium avium Complex (MAC) infection in HIV-infected patients. To determine the efficacy of daily versus weekly fluconazole for the prevention of deep fungal infections in this patient population.

SECONDARY: To determine the incidence of bacterial (including mycobacterial) infections, cryptosporidiosis, and toxoplasmosis in azithromycin versus non-azithromycin containing regimens. To determine the incidence of oropharyngeal and vaginal candidiasis in patients treated with daily versus weekly fluconazole. To compare survival and outcomes of primary endpoints in the treatment arms.

详细描述

Patients are randomized to receive azithromycin alone, rifabutin alone, or the two drugs in combination for MAC prophylaxis. Patients in each treatment group further receive one of two doses of concomitant fluconazole for deep fungal prophylaxis, unless specifically excluded for fluconazole randomization. Patients are followed for 1 to 2 years.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
Double

入排标准

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

入选标准

  • •Concurrent Medication:
  • •Preventive therapy with isoniazid for M. tuberculosis.
  • •Maintenance therapy for CMV retinitis.
  • •Patients must have:
  • •HIV infection or history of an AIDS-defining condition by CDC criteria.
  • •One documented CD4 count < 100 cells/mm3 within 12 months prior to study entry.
  • •NO active MAC disease, MAC bacteremia, or active mycobacterial infection (tuberculous or nontuberculous).
  • •NO acute opportunistic infection.
  • •Life expectancy of more than 6 months.
  • •Consent of parent or guardian if less than legal age of consent.

排除标准

  • •Co-existing Condition:
  • •Patients with the following symptoms or conditions are excluded:
  • •ALL PATIENTS -
  • •Unexplained fevers, elevation in alkaline phosphatase, pancytopenia, abnormal liver function tests, or odynophagia for which the diagnoses of MAC and fungal infections have not been excluded.
  • •Serious hypersensitivity reactions to macrolides or rifampin.
  • •Unable to tolerate oral medications. FOR FLUCONAZOLE RANDOMIZATION -
  • •Serious hypersensitivity reaction to fluconazole.
  • •Active fungal infection (cryptococcosis, histoplasmosis, blastomycosis, aspergillosis, Candida esophagitis, thrush, vaginal candidiasis).
  • •Positive baseline urine cryptococcal culture.
  • •Concurrent Medication:
  • •Excluded for fluconazole randomization:
  • •Maintenance therapy for deep fungal infections.
  • •Chronic therapy with ketoconazole or fluconazole.

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (12)

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