| Autor: |
Thomas P. Eisele, Immo Kleinschmidt, Sophie Sarrassat, Feiko terKuile, John M Miller, Javan Chanda, Kafula Silumbe, Aaron Samuels, Julia Janssen, Caroline Ogwang, John Bradley, Erica Orange, Josh Yukich, Ruth Ashton, Irene Kyomuhangi, Angela F Harris, Seydou Doumbia, Mahamoudou Toure, Mohamed Moumine, Silas Majambere, Monicah Mirai Mburu, Gift Mwaanga, Limonty Simubali, Edgar Simulundu, Adam Bennett, Laurence Slutsker, Gunter Muller, Eric Ochomo, John Gimnig, Paul C.D. Johnson, Joseph Wagman, Megan Littrell |
| Rok vydání: |
2022 |
| DOI: |
10.21203/rs.3.rs-1560370/v1 |
| Popis: |
BackgroundLong-lasting insecticidal nets (LLINs) and indoor residual spraying (IRS) target night-time indoor biting mosquitoes and effectively reduce malaria transmission in rural settings across Africa, but additional vector control tools are needed to interrupt transmission. Attractive targeted sugar baits (ATSBs) attract and kill mosquitoes, including those biting outdoors. Deployment of ATSBs incorporating the insecticide dinotefuran was associated with major reductions in mosquito density and longevity in Mali. The impact of this promising intervention on malaria transmission and morbidity now needs to be determined in a range of transmission settings.Methods/DesignWe will conduct three similar stand-alone, open-label, two-arm, cluster-randomized, controlled trials (cRCTs) in Mali, Kenya, and Zambia to determine the impact of ATSB + universal vector control versus universal vector control alone on clinical malaria. The trials will use a ‘fried-egg’ design, with primary outcomes measured in the core area of each cluster to reduce spill-over effects. All household structures in the ATSB clusters will receive two ATSBs, but the impact will be measured in the core of clusters. Restricted randomization will be used. The primary outcome is clinical malaria incidence among children aged 5-14 years in Mali and 1-14 years in Kenya and Zambia. A key secondary outcome is malaria parasite prevalence across all ages. The trials will include 76 clusters (38 per arm) in Mali and 70 (35 per arm) in each of Kenya and Zambia. The trials are powered to detect a 30% reduction in clinical malaria, requiring a total of 3,850 person-years of follow-up in Mali, 1,260 person-years in Kenya, and 1,610 person-years in Zambia. These sample sizes will be ascertained using two seasonal 8-month cohorts in Mali, and two 6-month seasonal cohorts in Zambia. In Kenya, which has year-round transmission, four 6-month cohorts will be used (total 24 months of follow-up). The design allows for one interim analysis in Mali and Zambia and two in Kenya.DiscussionStrengths of the design include: the use of multiple study sites with different transmission patterns and a range of vectors to improve external validity; a large number of clusters within each trial site; restricted randomization; between-cluster separation to minimize contamination between study arms; and an adaptive trial design. Noted threats to internal validity include: open-label design, risk of contamination between study arms, risk of imbalance of covariates across study arms, variation in durability of ATSB stations and potential disruption resulting from the COVID-19 pandemic.Trial registrationZambia: NCT04800055. Registration date: March 15, 2021 - https://clinicaltrials.gov/ct2/show/NCT04800055Mali: NCT04149119. Registration date: November 4, 2019 -https://clinicaltrials.gov/ct2/show/results/NCT04149119Kenya: NCT05219565. Registration date: February 2, 2022 - https://clinicaltrials.gov/ct2/show/NCT05219565 |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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