Protocol and statistical analysis plan for a randomized controlled trial of the effect of intravenous iron on anemia in Malawian pregnant women in their third trimester (REVAMP – TT)

R. Harding, E. Moya, Ricardo Ataíde, Z. Truwah, G. Mzembe, Gomezgani Mhango, Ayşe V. Demir, William Stones, Louise Randall, Marc Seal, Katherine Johnson, Stefan Bode, M. Mwangi, S. Pasricha, S. Braat, K. Phiri
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Abstract

Background: Anemia affects 40% of pregnant women globally, leading to maternal mortality, premature birth, low birth weight, and poor baby development. Iron deficiency causes over 40% of anemia cases in Africa. Oral iron supplementation is insufficient for Low-and-Middle-Income-Countries (LMICs) to meet current WHO targets. We hypothesized that a single intravenous dose of Ferric Carboxymaltose (FCM) may be more effective than oral iron treatment for anemia recovery, particularly in these settings where women present late for antenatal care. Methods: This is a two-arm parallel open-label individual-randomized controlled trial in third trimester, in malaria Rapid Diagnostic Test-negative pregnant women with moderate or severe anemia - capillary hemoglobin <10 g/dL – who are randomized to receive either parenteral iron – with FCM – or standard-of-care oral iron for the remainder of pregnancy. This is the sister trial to the second-trimester REVAMP trial, funded by the Bill and Melinda Gates Foundation (trial registration ACTRN12618001268235, Gates Grant number INV-010612). In REVAMP-TT, recruitment and treatment are performed within primary health centers. The trial will recruit 590 women across Zomba district, Malawi. The primary outcome is the proportion of anemic women - venous hemoglobin <11 g/dL - at 36 weeks’ gestation or delivery (whichever occurs first). Other pre-specified key secondary clinical and safety outcomes include maternal iron-status and hypophosphatemia, neonate birth weight, infant growth and infant iron and hematological parameters. Discussion: This study will determine whether FCM, delivered within primary health centers, is effective, safe and feasible for treating moderate to severe anemia in third-trimester pregnant Malawian women. This intervention could have long-term benefits for maternal and child health, resulting in improved survival and child development.
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马拉维妊娠晚期孕妇静脉注射铁治疗贫血的随机对照试验方案和统计分析计划(REVAMP - TT)
背景:贫血影响全球40%的孕妇,导致孕产妇死亡、早产、低出生体重和婴儿发育不良。非洲40%以上的贫血病例是缺铁造成的。口服补铁不足以使低收入和中等收入国家达到世卫组织目前的目标。我们假设单次静脉注射三羧基麦糖铁(FCM)可能比口服铁治疗对贫血恢复更有效,特别是在这些妇女产前护理较晚的情况下。方法:这是一项在妊娠晚期进行的双组平行开放标签个体随机对照试验,试验对象为疟疾快速诊断试验阴性、伴有中度或重度贫血(毛细血管血红蛋白<10 g/dL)的孕妇,她们被随机分为两组,一组接受含FCM的肠外铁治疗,另一组接受标准护理的口服铁治疗。这是由比尔和梅林达·盖茨基金会资助的中期REVAMP试验的姊妹试验(试验注册号ACTRN12618001268235,盖茨资助号INV-010612)。在REVAMP-TT项目中,招募和治疗在初级保健中心进行。该试验将在马拉维的Zomba地区招募590名妇女。主要结局是在妊娠36周或分娩时(以先发生者为准)贫血妇女静脉血红蛋白<11 g/dL的比例。其他预先指定的关键次要临床和安全性结果包括产妇铁状态和低磷血症、新生儿体重、婴儿生长和婴儿铁和血液学参数。讨论:本研究将确定在初级保健中心提供的FCM是否有效、安全和可行,用于治疗马拉维妊娠晚期妇女的中度至重度贫血。这一干预措施可能对孕产妇和儿童健康产生长期效益,从而改善生存和儿童发育。
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来源期刊
Gates Open Research
Gates Open Research Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
3.60
自引率
0.00%
发文量
90
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