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临床试验/NCT02721186
NCT02721186已完成不适用

Effectiveness of Mass Drug Administration (MDA) for Reducing Seasonal Malaria Transmission Towards Its Elimination in Hotspot Areas in Zanzibar - a Cluster-randomised Controlled Trial

Ulrika Morris1 个研究点 分布在 1 个国家目标入组 22,500 人开始时间: 2016年4月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
22,500
试验地点
1
主要终点
Cumulative notified malaria incidence in the MDA and control Shehias

研究概览

简要总结

The overall aim of this study is to determine the effectiveness of two rounds of mass drug administration (MDA) with dihydroartemisinin-piperaquine (DHAp) + single low dose (SLD) primaquine for reducing seasonal malaria transmission in Shehias considered hotspots on Unguja Island, Zanzibar.

详细描述

Study design: This is a cluster-randomised controlled study with two arms: an intervention arm with two rounds of MDA with dihydroartemisinin-piperaquine (DHAp) + single low dose (SLD) primaquine, and a control arm with no MDA.

Study site and study population: The study will be conducted in 16 hotspot Shehias (8 Shehias randomly allocated to each arm), in three districts (West, Central and South districts) in Unguja Island, Zanzibar. Hotspot Shehias [Shehia being the smallest administrative structure in Zanzibar] are defined as Shehias with an annual malaria incidence of >0.8%, calculated as the number of confirmed malaria infections notified at health facilities and during active case detection in 2015 / Shehia projected population for 2015. The study population will include all consenting residents of the selected Shehias, reaching approximately 24000 people.

Study implementation: Two rounds of MDA with DHAp (D-ARTEPP, Guilin Pharmaceutical (Shanghai) Co., Ltd., China) and SLD (0.25mg/kg) primaquine (Primaquine, Remedica Ltd.,Cyprus ) will be conducted approximately four weeks apart in the intervention Shehias, at the anticipated lowest point of malaria transmission prior to the onset of malaria transmission associated with the main rains in April-June 2016. The first drug dose including DHAp and SLD primaquine will be given under supervision whenever possible; the other two doses of the standard once daily DHAp regimen will be taken unsupervised at home. Labelled packets containing all three doses will be left with the head of household with clear instructions for individuals not present at the time of the household visit.

Study objectives: The primary objective of the study is to determine the effectiveness of two rounds of MDA with DHAp + SLD primaquine for reducing seasonal malaria transmission in Shehias considered hotspots on Unguja Island, Zanzibar. The secondary objectives of the study include determining MDA coverage, compliance, and safety after one and two rounds of DHAp + SLD primaquine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
6 Months 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Permanent or temporary resident of study Shehias (i.e., persons who stayed in the selected household the night before the interview)
  • Provision of informed consent (refusal must be recorded)
  • Age >6 months

排除标准

  • Women pregnant in first trimester (assessed by a specific set of questions designed to exclude pregnancy)
  • Severe disease that requires immediate referral to health facility or hospital
  • Concurrent antimalarial treatment at time of MDA or during the last 14 days
  • Inability to take oral medication
  • Additional exclusion criteria for treatment with SLD Primaquine:
  • Pregnancy (all trimesters, assessed by a specific set of questions designed to exclude pregnancy)
  • Women breast feeding infants aged < 6months

研究组 & 干预措施

MDA with DHAp and SLD Primaquine

Experimental

MDA will be conducted at two time points with an approximate four-week interval. All consenting and eligible community members will be administered age-appropriate treatment dose of dihydroartemisinin-piperaquine (D-ARTEPP, Guilin Pharmaceutical (Shanghai) Co., Ltd., China) and single low dose (0.25mg/kg) primaquine (Primaquine, Remedica Ltd., Cyprus) in house-to-house campaigns.

干预措施: MDA with DHAp and SLD Primaquine (Drug)

结局指标

主要结局

Cumulative notified malaria incidence in the MDA and control Shehias

时间窗: 6 months after second round of MDA

Cumulative notified malaria incidence determined as the number of confirmed malaria cases notified at health facilities (monitored through the malaria case notification system during the period of six months) over the Shehia population size determined by population enumeration at the time of the intervention.

次要结局

  • PCR determined community prevalence of Plasmodium infections in the MDA and control Shehias(Baseline and 3 months after second round of MDA)

研究者

发起方
Ulrika Morris
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ulrika Morris

Postdoc, Study Coordinator

Karolinska Institutet

研究点 (1)

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