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临床试验/NCT01417988
NCT01417988终止4 期

Prevention of Early Mortality by Presumptive TB Treatment in HIV-infected Patients Initiating Antiretroviral Therapy

Prof JMA Lange3 个研究点 分布在 3 个国家目标入组 44 人开始时间: 2011年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
发起方
入组人数
44
试验地点
3
主要终点
All-cause mortality in the first 24 weeks after initiation of ART

研究概览

简要总结

This study investigates the prevention of early mortality in patients initiating antiretroviral therapy (ART) in sub-Saharan Africa where 79% of the co-infected cases of TB reside. Many published studies have shown a surprisingly high proportion of all patients initiated on ART dying within 6 months (8-26%) with increasing risk with decreasing CD4 T cell count. The majority (median 70%) occur in the first 3 months with the greatest proportion of deaths due to previously undiagnosed tuberculosis (TB). The investigators will enroll patients from 4 geographically diverse countries (Gabon, Mozambique, South Africa, and Uganda) in a randomized open label clinical trial targeting a population of people with high mortality risk; patients with CD4 T cell count < 50 cells/μl and body mass index (BMI) < 18 kg/m2. Severely immunocompromised patients with low BMI in the intervention arm will receive presumptive anti-TB 4-drug chemotherapy and subsequently initiate ART within 2 weeks compared to ART alone. The main objective is to measure and compare early mortality in the group presumptively treated for TB in addition to ART. Other sub-objectives are to determine the predictors of early mortality and the causes of death by autopsy (traditional and verbal), to determine if presumptive anti-TB treatment affects viral suppression with ART, and to assess incidence rates and characterize drug toxicity in patients dually treated. Because of the high rates of TB co-infection in sub-Saharan Africa in the HIV-infected, the investigators expect that patients presumptively treated for TB in addition to HIV will have a lower mortality rate than patients receiving ART only. This trial is expected to be of great public health benefit and generalisability.

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
None

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

  • Aged > 18 years old
  • HIV-1 positive
  • Eligible for antiretroviral treatment with CD4 T cell count < 50 cells/μl
  • BMI < 18

排除标准

  • Patients with smear-positive pulmonary TB
  • Patients who fulfill the diagnostic criteria for smear-negative pulmonary or extrapulmonary TB (http://www.who.int/tb/publications/2006/tbhiv_recommendations.pdf ).
  • Previous TB treatment (history of TB medication for > 1 month
  • History of using antiretroviral drugs
  • Symptomatic known underlying liver disease or transaminases > 5x upper limit of normal
  • Known or suspected drug resistance to more than one first-line TB drug according to WHO criteria but excluding HIV infection (e.g. household contacts of MDRTB patients)
  • Pregnant or breast-feeding
  • Patients with cryptococcal meningitis (CrAG positive with neurologic symptoms)
  • Patients with other severe (opportunistic) disease such as disseminated KS, malignant lymphoma, toxoplasmosis who may not be able to tolerate anti-TB medication or require other specific therapy
  • Patients with danger signs (respiratory rate > 30 per minute, heart rate > 120bpm, temperature > 39oC, and unable to ambulate)
  • Taking other potentially life-saving medications (e.g. for other OIs, or immunosuppressants) that are incompatible with anti-TB chemotherapy or ART
  • Unable to swallow TB medications
  • Unable to follow-up at the clinic for regularly scheduled follow-up (e.g. too far from clinic)

研究组 & 干预措施

ART only arm

Active Comparator

ART (efavirenz-based) only (+ pyridoxine 50mg) given within 2 weeks after enrolment

干预措施: ART only arm (Drug)

结局指标

主要结局

All-cause mortality in the first 24 weeks after initiation of ART

时间窗: 24 weeks

次要结局

  • HIV viral suppression(24 weeks)
  • Causes of death(24 weeks)
  • TB incidence rates after ART initiation(24 weeks)
  • CD4 T cell absolute increase(24 weeks)
  • Safety and tolerability of anti-tuberculous medications(24 weeks)

研究者

发起方
Prof JMA Lange
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Prof JMA Lange

Executive Scientific Director AIGHD

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (3)

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