Prevention of Early Mortality by Presumptive TB Treatment in HIV-infected Patients Initiating Antiretroviral Therapy
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
- 否
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
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
Prof JMA Lange
Executive Scientific Director AIGHD
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
