Efficacy and safety of Ferrous iron on the prevention of Vascular cOgnitive impaiRment among patients with cerebral Infarction/TIA (FAVORITE): rationale and design of a multicentre randomised trial.

IF 2.6 1区 医学
Qian Jia, Peng Lei, Li Sun, Wei Li Jia, Yuesong Pan, Baoshi Yuan, Yinkai Wang, Qi Zhou, Xia Meng, Jing Jing, Jinxi Lin, Anxin Wang, Shuting Zhang, Zhen Hong, Yu Yang, Yunyun Xiong, Zixiao Li, Yilong Wang, Xingquan Zhao, Yongjun Wang
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引用次数: 0

Abstract

Background: The incidence of vascular cognitive impairment (VCI) is high in patients suffering from ischaemic stroke or transient ischaemic attack (TIA) or with vascular risk factors. Effective prevention strategies for VCI remain limited. Anaemia or low haemoglobin was found as an independent risk factor for adverse outcomes after acute stroke. Anaemia or low haemoglobin was possibly associated with an increased risk of poststroke cognitive impairment. Whether supplement of ferrous iron to correct anaemia reduces the risk of VCI and improves adverse outcomes in patients with ischaemic cerebrovascular disease remains uncertain.

Aim: We aim to introduce the design and rationale of the safety and efficacy of Ferrous iron on the prevention of Vascular cOgnitive impaiRment in patients with cerebral Infarction or TIA (FAVORITE) trial.

Design: FAVORITE is a randomised, placebo-controlled, double-blind, multicentre trial that compares supplement of ferrous iron with placebo for recent minor stroke/TIA patients complicated with mild anaemia or iron deficiency: Ferrous succinate sustained-release tablet 0.2 g (corresponding to 70 mg of elemental iron) once daily after or during breakfast for 12 weeks or placebo with much the same colour, smell and size as ferrous iron once daily during or after breakfast for 12 weeks. All paticipants will be followed within the next year.

Study outcomes: The primary effective outcome is the incidence of VCI at 3 months after randomisation and the primary safety outcome includes any gastrointestinal adverse event during 3 months.

Discussion: The FAVORITE trial will clarify whether supplement of ferrous iron to correct low haemoglobin reduces the risk of VCI in patients with recent ischaemic stroke or TIA complicated with mild anaemia or iron deficiency compared with placebo.

Trial registration number: NCT03891277.

亚铁预防脑梗塞/TIA 患者血管损伤的有效性和安全性(FAVORITE):多中心随机试验的原理和设计。
背景:缺血性中风或短暂性脑缺血发作(TIA)患者或有血管风险因素的患者中,血管性认知障碍(VCI)的发病率很高。有效预防血管性认知障碍的策略仍然有限。贫血或低血红蛋白是急性中风后不良预后的独立风险因素。贫血或低血红蛋白可能与中风后认知障碍风险增加有关。补充亚铁以纠正贫血是否能降低缺血性脑血管病患者发生 VCI 的风险并改善不良预后,目前仍不确定。目的:我们旨在介绍亚铁预防脑梗死或 TIA 患者血管性损伤的安全性和有效性试验(FAVORITE)的设计和原理:FAVORITE 是一项随机、安慰剂对照、双盲、多中心试验,旨在比较亚铁与安慰剂对近期并发轻度贫血或缺铁的轻微中风/TIA 患者的补充作用:琥珀酸亚铁缓释片 0.2 克(相当于 70 毫克铁元素),每天一次,在早餐后或早餐时服用,为期 12 周;或安慰剂,其颜色、气味和大小与亚铁大致相同,每天一次,在早餐时或早餐后服用,为期 12 周。所有参与者都将在未来一年内接受随访:主要有效结果是随机分组后 3 个月的 VCI 发生率,主要安全性结果包括 3 个月内的任何胃肠道不良事件:讨论:与安慰剂相比,FAVORITE 试验将明确补充亚铁以纠正低血红蛋白是否能降低近期缺血性中风或 TIA 并发轻度贫血或缺铁患者的 VCI 风险:NCT03891277.
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来源期刊
Journal of Investigative Medicine
Journal of Investigative Medicine MEDICINE, GENERAL & INTERNALMEDICINE, RESE-MEDICINE, RESEARCH & EXPERIMENTAL
自引率
0.00%
发文量
111
期刊介绍: Journal of Investigative Medicine (JIM) is the official publication of the American Federation for Medical Research. The journal is peer-reviewed and publishes high-quality original articles and reviews in the areas of basic, clinical, and translational medical research. JIM publishes on all topics and specialty areas that are critical to the conduct of the entire spectrum of biomedical research: from the translation of clinical observations at the bedside, to basic and animal research to clinical research and the implementation of innovative medical care.
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