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Evaluation of Long-Lasting Microbial Larvicides in Reducing Malaria Transmission and Clinical Malaria Incidence

Not Applicable
Completed
Conditions
Malaria
Interventions
Biological: Fourstar® granule, 90 day and 180 day briquettes Bti/Bs
Registration Number
NCT02392832
Lead Sponsor
University of California, Irvine
Brief Summary

In the past decade, massive scale-up of insecticide-treated nets (ITN) and indoor residual spraying (IRS), together with the introduction of artemisinin-combination treatments, have led to substantial reductions in malaria prevalence and incidence in African highlands. However, rising insecticide resistance and increased outdoor transmission have greatly hampered the effectiveness of ITN and IRS because the current indoor-based interventions do not target the outdoor-biting mosquitoes. Therefore, new supplemental interventions that can tackle outdoor transmission and pyrethroid insecticide resistance are urgently needed. The central objective of this study is to determine the efficacy and cost-effectiveness of EPA-approved long-lasting microbial larvicides in reducing malaria transmission and clinical malaria incidence in western Kenya highlands.

Detailed Description

In the past decade, massive scale-up of insecticide-treated nets (ITNs) and indoor residual spraying (IRS), together with the use of artemisinin combination treatments, have led to major changes in malaria epidemiology and vector biology. Along with the significant reduction in overall malaria prevalence and incidence, extensive use of insecticides has created large selection pressures for resistance in the malaria vector populations and for potential outdoor transmission, which appears to be limiting the success of ITNs and IRS. Because IRS and ITN have little impact on outdoor resting and early biting vectors, outdoor transmission represents one of the most important challenges in malaria control. Therefore, new interventions that can augment the current public health measures to reduce outdoor transmission are urgently needed. Larval control has historically been very successful and is widely used for mosquito control in many parts of the world, except in Africa. Factors limiting the use of larvicides include high costs associated with frequent habitat re-treatment. Now a new US EPA-approved long-lasting formulation, potentially effective for 6 months is available. The central objective of this study is to determine the effect of long-lasting microbial larviciding on the incidence of clinical malaria and reduction of transmission intensity. Our hypothesis is that addition of long-lasting microbial larviciding to ongoing ITN and IRS programs will lead to significant reductions in both indoor and outdoor malaria transmission and malaria incidence.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
240000
Inclusion Criteria
  • All clinical malaria cases from participated local hospitals and clinics.
Exclusion Criteria
  • Infants younger than 6 months.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Intervention armFourstar® granule, 90 day and 180 day briquettes Bti/BsFourstar® granule formulation, 90day and 180 day briquettes Bti/Bs in larval habitats of malaria vectors.
Primary Outcome Measures
NameTimeMethod
Changes in clinical malaria incidence ratebaseline and 4 months following the interventions

Human population for each site stratified into three age groups, under 5 years, 6-15 years and \>15 years, will be ascertained from our existing demographic database. Age group level aggregate morbidity data with number of clinical malaria cases without any identifiers will be obtained from local hospitals and clinics where the study residents seek treatment. This data is reported to the Ministry of Health of Kenya and hence, is publicly available.

Secondary Outcome Measures
NameTimeMethod
Changes in vector abundancebaseline and 4 months following the interventions

Malaria vector abundance is measured by the total density of An. gambiae, An. arabiensis, An. funestus and other Anopheles species capable of transmitting malaria, collected indoors and outdoors by the CO2-baited CDC light trap, 64 trap nights in each of indoor and outdoor environments per site per month. Malaria transmission intensity is measured by the sum of indoor and outdoor entomological inoculation rate (EIR).

EIRbaseline and 4 months following the interventions

Malaria transmission intensity is measured by the sum of indoor and outdoor entomological inoculation rate (EIR).

Trial Locations

Locations (1)

Kenya Medical Research Institute

🇰🇪

Kisumu, Kenya

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