PACTR2008060000861040已完成未知
An international multicentre controlled clinical trial to evaluate high dose rifapentine and a quinolone in the treatment of pulmonary tuberculosis
St Georges Hospital Medical School trading as St Georges University of London0 个研究点目标入组 1,100 人开始时间: 2008年2月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 1,100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Newly diagnosed pulmonary tuberculosis
- •2. Two sputum specimens positive for tubercle bacilli on direct smear microscopy
- •3. Either no previous anti-tuberculosis chemotherapy, or less than two weeks of previous chemotherapy
- •4. Aged 18 years and over
- •5. A firm home address that is readily accessible for visiting and be intending to remain there during the entire treatment and follow up period
- •6. Willing to agree to participate in the study and to give a sample of blood for HIV testing
排除标准
- •1. Has any condition (except HIV infection) that may prove fatal during the study period
- •2. Has Tuberculous (TB) meningitis
- •3. Has pre-existing non-tuberculous disease likely to prejudice the response to, or assessment of, treatment e.g., insulin-dependent diabetes, liver or kidney disease, blood disorders, peripheral neuritis
- •4. Is female and known to be pregnant, or breast feeding
- •5. Is suffering from a condition likely to lead to uncooperative behaviour such as psychiatric illness or
研究者
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