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临床试验/NCT05150808
NCT05150808Unknown3 期

WHO Phase III Evaluation of Vectron T500 (Broflanilide 50WP) for IRS in Tanzania

London School of Hygiene and Tropical Medicine2 个研究点 分布在 2 个国家目标入组 12,500 人开始时间: 2020年10月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
入组人数
12,500
试验地点
2
主要终点
Entomological inoculation rate EIR

研究概览

简要总结

Malaria is a major public health problem in Africa. An important way to control the disease is by Indoor Residual Spraying of insecticide in houses. Insecticide resistance has become a major problem. This trial will evaluate a novel insecticide against those insecticide resistant mosquito vectors in Tanzania E Africa.

详细描述

Background: Indoor residual spraying (IRS) is one of the major methods of malaria vector control across sub-Saharan Africa, responsible for reducing malaria incidence by 10% since 2000. However, effective vector control is increasingly threatened by the rapid spread of insecticide resistance. Consequently, there have been investments in the development of new insecticides for IRS that possess novel modes of action with long residual activity, low mammalian and environmental toxicity and minimal cross-resistance. VECTRONTM T500, a new IRS insecticide containing the active ingredient broflanilide 50% WP, has been shown to be efficacious against both pyrethroid-susceptible and -resistant vector strains on mud and concrete substrates in phase II experimental hut trials in Tanzania.

Method: A two-arm non-inferiority cluster randomized controlled trial will be conducted in Muheza District, Tanga Region, Tanzania. VECTRONTM T500 will be compared to the IRS formulation Fludora® Fusion (active ingredients: clothianidin 50% WP + deltamethrin 6.25% WP). The predominant malaria vectors in the study area are pyrethroid-resistant Anopheles gambiae s.s., An. arabiensis and An. funestus s.s. Sixteen selected clusters of 75-200 households in each cluster will be pair-matched on baseline vector densities and allocated to reference and intervention arms. Consenting households in the intervention arm will be sprayed with VECTRONTM T500 and those in the reference arm will receive Fludora® Fusion. Monthly CDC light traps will collect mosquitoes to determine vector density, indoor biting, sporozoite and entomological inoculation rates (EIR). Phenotypic resistance to IRS active ingredients will be assessed using CDC bottle bioassays. Molecular and metabolic resistance mechanisms will be characterised among Anopheles field populations from both trial arms. Residual efficacy of both brands of insecticide will be monitored for 12 months post-spraying. A semi-structured questionnaire and focus group discussions will explore social and cultural factors that influence acceptability, perceived adverse effects and benefits of IRS.

Discussion: This protocol describes a phase III non-inferiority evaluation of a novel IRS product to reduce the density and EIR of pyrethroid-resistant Anopheles vectors. If VECTRONTM T500 proves non-inferior to Fludora® Fusion, it may be considered as an additional vector control product for malaria prevention and insecticide resistance management schemes.

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
Double (Participant, Care Provider)

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

  • All households who consent to IRS malaria control

排除标准

  • 未提供

研究组 & 干预措施

Intervention IRS

Active Comparator

Intervention IRS insecticide will be sprayed on the walls and ceilings of 8 clusters

干预措施: IRS insecticide: Vectron T500 (Other)

Control IRS

Active Comparator

WHO approved IRS insecticide will be sprayed on the walls and ceilings of 8 clusters

干预措施: IRS insecticide: Vectron T500 (Other)

结局指标

主要结局

Entomological inoculation rate EIR

时间窗: 12-15 months

Reduction in EIR

Vector density

时间窗: 12-15 months

Reduction in vector population density

Sporozoite rate

时间窗: 12-15 months

Reduction in sporozoite rate

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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