Trial | NCT02721186  Report issue

Title

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

  • Phase

    N/A

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    22500
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.
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.
Study Started
Apr 30
2016
Primary Completion
Dec 31
2016
Study Completion
Sep 30
2017
Last Update
Oct 05
2017

Drug MDA with DHAp and SLD Primaquine

  • Other names: Mass drug administration with DHAp and SLD Primaquine, MDA with Dihydroartemisinin-Piperaquine and SLD Primaquine, MDA with D-ARTEPP and single low dose Primaquine

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.

Control No Intervention

The control arm (no MDA) will have the standard care offered by the Ministry of Health and Social welfare which applies to both arms. This includes passive case detection of individuals seeking treatment at local health facilities, and universal coverage of long lasting insecticide treated bed nets and indoor residual spraying in the study areas.

Criteria 

Inclusion Criteria:

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

Exclusion Criteria:

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
No Results Posted