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首页> 外文期刊>The Lancet >Antiretroviral prophylaxis for HIV infection in injecting drug users in Bangkok, Thailand (the BangkokTenofovir Study): a randomised, double-blind, placebo-controlled phase 3 trial
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Antiretroviral prophylaxis for HIV infection in injecting drug users in Bangkok, Thailand (the BangkokTenofovir Study): a randomised, double-blind, placebo-controlled phase 3 trial

机译:泰国曼谷注射吸毒者的抗逆转录病毒预防HIV感染(曼谷替诺福韦研究):一项随机,双盲,安慰剂对照的3期试验

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Background Antiretroviral pre-exposure prophylaxis reduces sexual transmission of HIV. We assessed whether daily oral use of tenofovir disoproxil fumarate (tenofovir), an antiretroviral, can reduce HIV transmission in injecting drug users.Methods In this randomised, double-blind, placebo-controlled trial, we enrolled volunteers from 17 drug-treatment clinics in Bangkok, Thailand. Participants were eligible if they were aged 20-60 years, were HIV-negative, and reported injecting drugs during the previous year. We randomly assigned participants (1:1; blocks of four) to either tenofovir or placebo using a computer-generated randomisation sequence. Participants chose either daily directly observed treatment or monthly visits and could switch at monthly visits. Participants received monthly HIV testing and individualised risk-reduction and adherence counselling, blood safety assessments every 3 months, and were offered condoms and methadone treatment. The primary efficacy endpoint was HIV infection, analysed by modified intention-to-treat analysis. This trial is registered with ClinicalTrials.gov, number NCT00119106.Findings Between June 9, 2005, and July 22, 2010, we enrolled 2413, participants, assigning 1204 to tenofovir and 1209 to placebo.
机译:背景技术抗逆转录病毒暴露前预防可减少HIV的性传播。我们评估了每天口服口服抗逆转录病毒药物替诺福韦富马酸替诺福韦(tenofovir)是否可以减少注射吸毒者的HIV传播。方法在这项随机,双盲,安慰剂对照试验中,我们招募了来自17家药物治疗诊所的志愿者泰国曼谷。如果参与者年龄在20至60岁之间,艾滋病毒呈阴性,并且在上一年报告了注射药物,则有资格参加。我们使用计算机生成的随机序列将参与者(1:1;四人一组)随机分配给替诺福韦或安慰剂。参与者选择每日直接观察治疗或每月就诊,并且可以在每月就诊时切换。参加者每月接受一次艾滋病毒检测,并每三个月进行个性化的降低风险和依从性咨询,血液安全评估,并接受安全套和美沙酮治疗。主要功效终点是HIV感染,可通过改良的意向治疗分析进行分析。该试验已在ClinicalTrials.gov上注册,编号为NCT00119106。发现在2005年6月9日至2010年7月22日期间,我们招募了2413名参与者,将1204分配给替诺福韦和1209分配给安慰剂。

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