...
首页> 外文期刊>BMC Infectious Diseases >Repeated doses of Praziquantel in Schistosomiasis Treatment (RePST) – single versus multiple praziquantel treatments in school-aged children in C?te d’Ivoire: a study protocol for an open-label, randomised controlled trial
【24h】

Repeated doses of Praziquantel in Schistosomiasis Treatment (RePST) – single versus multiple praziquantel treatments in school-aged children in C?te d’Ivoire: a study protocol for an open-label, randomised controlled trial

机译:在血吸虫病治疗(REPST)的重复剂量的吡喹酮(REPST) - 单一对幼儿儿童的多种吡喹酮治疗C?TE D'IVOIRE:一个开放标签,随机对照试验的研究方案

获取原文
           

摘要

Large scale administration of the anthelminthic drug praziquantel (PZQ) to at-risk populations is the cornerstone of schistosomiasis control, although persisting high prevalence of infections in some areas and growing concerns of PZQ resistance have revealed the limitations of this strategy. Most studies assessing PZQ efficacy have used relatively insensitive parasitological diagnostics, such as the Kato-Katz (KK) and urine-filtration methods, thereby overestimating cure rates (CRs). This study aims to determine the efficacy of repeated PZQ treatments against Schistosoma mansoni infection in school-aged children in C?te d'Ivoire using the traditional KK technique, as well as more sensitive antigen- and DNA-detection methods. An open-label, randomised controlled trial will be conducted in school-aged children (5 to 18?years) from the region of Taabo, C?te d'Ivoire, an area endemic for S. mansoni. This 8-week trial includes four two-weekly standard doses of PZQ in the "intense treatment" intervention group and one standard dose of PZQ in the "standard treatment" control group. The efficacy of PZQ will be evaluated in stool samples using the KK technique and real-time PCR as well as in urine using the point-of-care circulating cathodic antigen test and the up-converting phosphor, lateral flow, circulating anodic antigen assay. The primary outcome of the study will be the difference in CR of intense versus standard treatment with PZQ on individuals with a confirmed S. mansoni infection measured by KK. Secondary outcomes include the difference in CR and intensity reduction rate between the intense and standard treatment groups as measured by the other diagnostic tests, as well as the accuracy of the different diagnostic tests, and the safety of PZQ. This study will provide data on the efficacy of repeated PZQ treatment on the clearance of S. mansoni as measured by several diagnostic techniques. These findings will inform future mass drug administration policy and shed light on position of novel diagnostic tools to evaluate schistosomiasis control strategies. The study is registered at EudraCT (2016-003017-10, date of registration: 22 July 2016) and ( NCT02868385 , date of registration: 16 August 2016).
机译:大规模施用Anthelminthic药物Praziquantel(PZQ)到风险群体是血吸虫病控制的基石,尽管在某些领域的感染率高,但PZQ抗性的日益令人担忧揭示了这种策略的局限性。评估PZQ疗效的大多数研究使用了相对不敏感的寄生虫学诊断,例如Kato-Katz(KK)和尿液过滤方法,从而估计固化率(CRS)。本研究旨在利用传统的KK技术确定在C-TE D'Ivoire中的学龄儿童血吸虫曼逊感染对血吸虫瘤感染的疗效,以及更敏感的抗原和DNA检测方法。将在Tabo地区(C-Te D'Ivoire)区域,在塔博地区(5至18岁)在塔博地区,这是一个开放标签,随机对照审判,C-TE D'IVOIRE,S. Mansoni的区域。该8周试验包括“强烈治疗”干预组中的四个两周标准剂量的PZQ,并在“标准治疗”对照组中的一种标准剂量的PZQ。使用KK技术和实时PCR以及使用护理点循环阴极抗原试验和上转换磷光体,循环阳极抗原测定,在粪便样品中以及尿液中的粪便中的疗效。该研究的主要结果将是患有KK测量的确认的S. Mansoni感染的PZQ对PZQ的强烈与标准治疗的差异。二次结果包括通过其他诊断测试测量的强烈和标准治疗组之间Cr和强度降低率的差异,以及不同诊断测试的准确性以及PZQ的安全性。本研究将提供关于通过几种诊断技术测量的重复PZQ处理对S. Mansoni的间隙的疗效的数据。这些调查结果将通知未来的大众药物管理政策,并揭示新型诊断工具的位置,以评估血吸虫病控制策略。该研究在Eudract注册(2016-003017-10,日期(2016-003017-10):2016年7月22日)和(NCT02868385,日期(注册):2016年8月16日)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号