Real-World Effectiveness of the R21/Matrix-M Malaria Vaccine in Children in Burkina Faso and Uganda
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 20,000
- 试验地点
- 21
- 主要终点
- Dose-specific effectiveness of R21/Matrix-M against microscopy-confirmed clinical malaria
研究概览
简要总结
The AVERT study is a prospective observational test-negative case control study evaluating the real-world effectiveness of the R21/Matrix-M malaria vaccine among children younger than 5 years in Burkina Faso and Uganda. Children who seek outpatient care with suspected malaria and are eligible for the national R21/Matrix-M vaccination program will be enrolled. Malaria infection will be determined by blood smear microscopy. Children with a positive microscopy result will be classified as cases and children with a negative result as controls. Vaccination history, including the number and timing of doses, will be obtained primarily from vaccination cards or other written records. Vaccine effectiveness will be estimated by comparing the odds of vaccination among cases and controls.
详细描述
R21/Matrix-M has been introduced through national immunization programs, but its effectiveness under routine conditions may differ from efficacy observed in clinical trials because children may receive different numbers of doses, doses may be delayed, protection may wane, and malaria transmission and other prevention measures vary across settings.
AVERT will use a prospective test-negative case-control design at approximately 22 outpatient health facilities in moderate- to high-transmission areas of Burkina Faso and Uganda. Consecutive children younger than 5 years who meet country definitions for suspected malaria, are eligible for R21/Matrix-M vaccination, and have caregiver consent will be enrolled. All participants will undergo malaria testing as part of routine care, with study blood smear microscopy used to assign case or control status. A structured caregiver questionnaire will collect demographic, clinical, residential, socioeconomic, health-care access, and malaria-prevention information. R21/Matrix-M dose number and vaccination dates will be verified primarily from vaccination cards, individual health records, or facility vaccination registers.
Cases and controls will be matched, when feasible, by geographic area and calendar time. Conditional or standard logistic regression will estimate adjusted odds ratios comparing vaccinated and unvaccinated children, and vaccine effectiveness will be calculated as (1 - adjusted odds ratio) x 100%. Analyses will be conducted separately by country and will assess effectiveness by dose, time since vaccination, dose spacing, transmission intensity, sex, and use of seasonal malaria chemoprevention, insecticide-treated nets, and indoor residual spraying. A health-system-perspective economic evaluation will estimate incremental cost per uncomplicated clinical malaria case averted.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 5 Months 至 5 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Residence in an area where R21/Matrix-M is implemented and within the catchment area of a selected study facility.
- •Younger than 5 years and eligibleto receive R21/Matrix-M under the national vaccination schedule at rollout.
- •Meets the country definition of suspected malaria, generally axillary temperature of at least 37.5 degrees Celsius or a history of fever within the previous 24 hours, and is undergoing malaria testing.
- •Written informed consent provided by an adult caregiver aged 18 years or older.
排除标准
- •Caregiver is unable or unwilling to provide informed consent.
- •Severe non-malaria illness at presentation that would interfere with study participation.
- •Repeat presentation within the protocol-defined exclusion window after a previous enrollment: within 14 days after a microscopy-positive visit; or more than 7 but fewer than 14 days after a microscopy-negative visit. A microscopy-negative visit followed by a positive diagnosis within 7 days will be reclassified as positive rather than treated as a new enrollment.
- •Documented receipt of any RTS,S malaria vaccine dose.
研究组 & 干预措施
Suspected malaria cases that test positive using microscopy
Eligible children with suspected malaria whose enrollment blood smear microscopy result is positive for P. falciparum infection
干预措施: R21/Matris-M Malaria vaccine (Biological)
Suspected malaria cases that test negative using microscopy
Eligible children with suspected malaria whose enrollment blood smear microscopy result is negative for P. falciparum infection
干预措施: R21/Matris-M Malaria vaccine (Biological)
结局指标
主要结局
Dose-specific effectiveness of R21/Matrix-M against microscopy-confirmed clinical malaria
时间窗: At the enrollment illness episode, during the approximately 7- to 8-month study recruitment period
Adjusted vaccine effectiveness will be calculated as (1 - adjusted odds ratio) x 100%. The odds ratio will compare the odds of each documented R21/Matrix-M dose category among microscopy-positive malaria cases with the odds among microscopy-negative controls, using children with 0 doses as the primary reference group. Prespecified grouped dose categories will be used if individual dose categories do not have adequate statistical power.
次要结局
- Effectiveness according to vaccine dose timing(At the enrollment illness episode, during the approximately 7- to 8-month recruitment period)
- Effectiveness of R21/Matrix-M by time since vaccination(At the enrollment illness episode, during the approximately 7- to 8-month recruitment period)
- Effect modification of vaccine effectiveness by malaria transmission intensity(At the enrollment illness episode, during the approximately 7- to 8-month recruitment period)
- Effect modification of vaccine effectiveness by sex(At the enrollment illness episode, during the approximately 7- to 8-month recruitment period)
- Effect modification by other malaria prevention interventions(At the enrollment illness episode, during the approximately 7- to 8-month recruitment period)
- Effectiveness of the fourth dose relative to the three-dose primary series(At the enrollment illness episode, during the approximately 7- to 8-month recruitment period)