Barcelona Institute for Global Health, Hospital Clinic-University of Barcelona, Barcelona, Spain.
Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Trials. 2024 Sep 27;25(1):626. doi: 10.1186/s13063-024-08443-9.
Azithromycin has been shown to be beneficial in preventing infectious diseases, including malaria, infectious diarrhoea and pneumonia. A cluster randomised control trial on azithromycin MDA in children in Niger, Malawi and Tanzania found a reduction in all-cause under-five (U5) mortality in communities who received azithromycin compared to placebo. However, the reduction was largest and statistically significant only in Niger. The purpose of this trial is to evaluate the impact of azithromycin plus intermittent preventive treatment in infants (IPTi), recently renamed by the World Health Organisation as perennial malaria chemoprevention (PMC), with sulfadoxine-pyrimethamine (SP) on all-cause mortality up to 18 months of age in children living in areas of high mortality burden through the Expanded Program on Immunisation (EPI) in Sierra Leone.
The Improving Care through Azithromycin Research for Infants in Africa (ICARIA) trial is a phase III two-arm, individually randomised, double-blinded, placebo-controlled trial administering oral AZI (20 mg/kg bodyweight) at three time points to children attending EPI visits in Sierra Leone. A total of 20,560 infants attending the first EPI contact at around 6 weeks of age are recruited and randomised to AZI or placebo in a 1:1 ratio. The second and third AZI/placebo doses are given at 9 and 15 months of age. The primary outcome of the trial is all-cause mortality rate at 18 months of age assessed through mortality surveillance. Other trial outcomes include the impact on antimicrobial resistance, and on the immune response to certain key routine EPI immunisations, the safety of the intervention, the prevalence of SP resistance markers and the feasibility, and acceptability of adding AZI to the EPI programme.
The trial will provide the evidence needed to inform policy regarding the adoption and large-scale implementation of AZI in areas of high-mortality burden in sub-Saharan Africa.
ClinicalTrials.gov NCT04235816. Registered on 22 January 2020. Pan-African Clinical Trials Registry PACTR202004540256535. Registered on 14 April 2020.
阿奇霉素已被证明可预防包括疟疾、感染性腹泻和肺炎在内的传染病。在尼日尔、马拉维和坦桑尼亚开展的一项针对儿童的阿奇霉素大规模推广使用(MDA)的整群随机对照试验发现,与安慰剂相比,接受阿奇霉素治疗的社区五岁以下儿童(U5)全因死亡率有所下降。然而,这种降幅在尼日尔最大且具有统计学意义。本试验旨在评估阿奇霉素联合间歇性预防治疗在婴儿(IPTi)中的作用,世界卫生组织最近将其重新命名为常年疟疾化学预防(PMC),与磺胺多辛-乙胺嘧啶(SP)联合应用对生活在高死亡率负担地区的儿童(通过扩大免疫规划(EPI)在塞拉利昂)18 个月内的全因死亡率的影响。
改善非洲婴儿阿奇霉素治疗效果研究(ICARIA)试验是一项三期、双盲、安慰剂对照、两臂、个体随机临床试验,对在塞拉利昂参加 EPI 就诊的儿童在三个时间点口服阿奇霉素(20mg/kg 体重)。共有 20560 名 6 周龄左右首次参加 EPI 接触的婴儿被招募并以 1:1 的比例随机分为阿奇霉素组或安慰剂组。第二次和第三次阿奇霉素/安慰剂剂量分别在 9 个月和 15 个月时给予。试验的主要结局是通过死亡率监测评估 18 个月时的全因死亡率。其他试验结局包括对抗生素耐药性的影响,以及对某些关键常规 EPI 免疫接种的免疫反应、干预措施的安全性、SP 耐药标志物的流行情况以及将阿奇霉素纳入 EPI 计划的可行性和可接受性。
该试验将提供必要的证据,为在撒哈拉以南非洲高死亡率地区采用和大规模实施阿奇霉素提供依据。
ClinicalTrials.gov NCT04235816。于 2020 年 1 月 22 日注册。泛非临床试验注册中心 PACTR202004540256535。于 2020 年 4 月 14 日注册。