首页> 外文期刊>BMC Infectious Diseases >Protocol, rationale and design of PEOPLE (Post ExpOsure Prophylaxis for LEprosy in the Comoros and Madagascar): a cluster randomized trial on effectiveness of different modalities of implementation of post-exposure prophylaxis of leprosy contacts
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Protocol, rationale and design of PEOPLE (Post ExpOsure Prophylaxis for LEprosy in the Comoros and Madagascar): a cluster randomized trial on effectiveness of different modalities of implementation of post-exposure prophylaxis of leprosy contacts

机译:人的议定书,理由和设计(Comoros和Madagascar的麻风病后预防性):一组随机试验,了解不同方式的曝光后触发后的不同方式的效果

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BACKGROUND:Leprosy is an ancient infectious disease with a global annual incidence that has plateaued above 200,000 new cases since over a decade. New strategies are required to overcome this stalemate. Post-exposure prophylaxis (PEP) with a single dose of Rifampicin (SDR) has conditionally been recommended by the World Health Organization (WHO), based on a randomized-controlled-trial in Bangladesh. More evidence is required. The Post ExpOsure Prophylaxis for Leprosy (PEOPLE) trial will assess effectiveness of different modalities of PEP on the Comoros and Madagascar.METHODS:PEOPLE is a cluster-randomized trial with villages selected on previous leprosy-incidence and randomly allocated to four arms. Four annual door-to-door surveys will be performed in all arms. All consenting permanent residents will be screened for leprosy. Leprosy patients will be treated according to international guidelines and eligible contacts will be provided with SDR-PEP. Arm-1 is the comparator in which no PEP will be provided. In arms 2, 3 and 4, SDR-PEP will be provided at double the regular dose (20?mg/kg) to eligible contacts aged two years and above. In arm 2 all household-members of incident leprosy patients are eligible. In arm 3 not only household-members but also neighbourhood contacts living within 100-m of an incident case are eligible. In arm 4 such neighbourhood contacts are only eligible if they test positive to anti-PGL-I, a serological marker. Incidence rate ratios calculated between the comparator arm 1 and each of the intervention arms will constitute the primary outcome.DISCUSSION:Different trials on PEP have yielded varying results. The pivotal COLEP trial in Bangladesh showed a 57% reduction in incidence over a two-year period post-intervention without any rebound in the following years. A study in a high-incidence setting in Indonesia showed no effect of PEP provided to close contacts but a major effect of PEP provided as a blanket measure to an entire island population. High background incidence could be the reason of the lack of effect of PEP provided to individual contacts. The PEOPLE trial will assess effectiveness of PEP in a high incidence setting and will compare three different approaches, to identify who benefits most from PEP.TRIAL REGISTRATION:Clinicaltrials.Gov. NCT03662022. Initial Protocol Version 1.2, 27-Aug-2018.
机译:背景:麻风病是一种古代传染病,其全球性年发病率,自十年来以来已经高于20万人的新案件。克服这种僵局需要新的策略。曝光后预防(PEP)具有一剂利福平(SDR),由世界卫生组织(世卫组织)根据孟加拉国的随机控制试验有条件地推荐了一定剂量的利福平(SDR)。需要更多的证据。暴露后暴露的麻风病(人)审判的预防将评估Comoros和Madagascar的不同方式的效果。方法:人们是与以前的麻风病发生率上选择的村庄的群体随机试验,并随机分配给四个武器。在所有武器中都会进行四个每年的门到门调查。所有同意永久性居民都将被筛查麻风病。麻风病患者将根据国际指南进行处理,并将提供SDR-PEP的合格联系。 ARM-1是其中没有PEP的比较器。在武器2,3和4中,SDR-PEP将以双重定期剂量(20μmg/ kg)提供给符合两年及以上的符合条件的联系人。在ARM 2中,所有事故麻风病患者的家庭成员都有资格。在ARM 3中不仅家庭成员,而且还有居住在100米的事件案件中的邻近联系是符合条件的。在ARM 4中,这种邻域触点只能符合条件,如果它们测试抗PGL-I,血清学标记。比较器臂1和每个干预臂之间计算的发病率比将构成主要的结果。探讨:PEP上的不同试验产生了不同的结果。孟加拉国的关键课程审判审判在干预后期后发病率降低了57%,而不再在持续的几年内反弹。在印度尼西亚的高发生率环境中的一项研究表明,PEP提供的效果以关闭接触,但PEP作为整个岛屿群体的毯子尺寸提供了重大影响。高背景发生率可能是缺乏PEP提供给个别联系的原因。人民试验将评估PEP在高发型环境中的有效性,并将比较三种不同的方法,以确定谁来自PEP.Trial注册:ClinicalTrials.gov。 nct03662022。初始协议版本1.2,278-2018。

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