Medical Research Council (MRC) Unit The Gambia at London School of Hygiene & Tropical Medicine (LSHTM), PO Box 273, Fajara, Banjul, The Gambia.
Division of Human Nutrition and Health, Wageningen University, PO Box 17, 6700, AA, Wageningen, The Netherlands.
Trials. 2024 Apr 19;25(1):270. doi: 10.1186/s13063-024-08101-0.
The World Health Organization recommends universal iron supplementation for children aged 6-23 months in countries where anaemia is seen in over 40% of the population. Conventional ferrous salts have low efficacy due to low oral absorption in children with inflammation. Haem iron is more bioavailable, and its absorption may not be decreased by inflammation. This study aims to compare daily supplementation with haem iron versus ferrous sulphate on haemoglobin concentration and serum ferritin concentration after 12 weeks of supplementation.
This will be a two-arm, randomised controlled trial. Gambian children aged 6-12 months with anaemia will be recruited within a predefined geographical area and recruited by trained field workers. Eligible participants will be individually randomised using a 1:1 ratio within permuted blocks to daily supplementation for 12 weeks with either 10.0 mg of elemental iron as haem or ferrous sulphate. Safety outcomes such as diarrhoea and infection-related adverse events will be assessed daily by the clinical team (see Bah et al. Additional file 4_Adverse event eCRF). Linear regression will be used to analyse continuous outcomes, with log transformation to normalise residuals as needed. Binary outcomes will be analysed by binomial regression or logistic regression, Primary analysis will be by modified intention-to-treat (i.e., those randomised and who ingested at least one supplement dose of iron), with multiple imputations to replace missing data. Effect estimates will be adjusted for baseline covariates (C-reactive protein, alpha-1-acid glycoprotein, haemoglobin, ferritin, soluble transferrin receptor).
This study will determine if therapeutic supplementation with haem iron is more efficacious than with conventional ferrous sulphate in enhancing haemoglobin and ferritin concentrations in anaemic children aged 6-12 months.
Pan African Clinical Trial Registry PACTR202210523178727.
世界卫生组织建议在贫血发病率超过 40%的国家,为 6-23 个月大的儿童普遍补充铁元素。对于存在炎症的儿童,常规的亚铁盐由于口服吸收率低,疗效较低。血红素铁的生物利用度更高,其吸收可能不会因炎症而减少。本研究旨在比较 12 周补充血红素铁与硫酸亚铁对血红蛋白浓度和血清铁蛋白浓度的影响。
这将是一项双臂、随机对照试验。在预先设定的地理区域内招募患有贫血的 6-12 个月大的冈比亚儿童,并由经过培训的现场工作人员招募。合格的参与者将在排列块内以 1:1 的比例进行个体随机分组,接受为期 12 周的每日补充治疗,分别使用 10.0 毫克元素铁的血红素或硫酸亚铁。临床团队将每天评估安全性结果,如腹泻和感染相关的不良事件(见 Bah 等人,附加文件 4_不良事件 eCRF)。线性回归将用于分析连续结果,需要时对数转换使残差正态化。二项结果将通过二项回归或逻辑回归进行分析,主要分析将采用修改后的意向治疗(即随机分组且至少摄入一剂铁补充剂的患者),并进行多重插补以替换缺失数据。效应估计值将根据基线协变量(C 反应蛋白、α-1-酸性糖蛋白、血红蛋白、铁蛋白、可溶性转铁蛋白受体)进行调整。
本研究将确定在 6-12 个月大的贫血儿童中,血红素铁的治疗性补充是否比常规硫酸亚铁更能有效提高血红蛋白和铁蛋白浓度。
泛非临床试验注册中心 PACTR202210523178727。