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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.
Jia, Qian; Lei, Peng; Sun, Li; Jia, Wei Li; Pan, Yuesong; Yuan, Baoshi; Wang, Yinkai; Zhou, Qi; Meng, Xia; Jing, Jing; Lin, Jinxi; Wang, Anxin; Zhang, Shuting; Hong, Zhen; Yang, Yu; Xiong, Yunyun; Li, Zixiao; Wang, Yilong; Zhao, Xingquan; Wang, Yongjun.
Afiliação
  • Jia Q; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Lei P; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Sun L; Department of Neurology and State Key Laboratory of Biotherapy, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
  • Jia WL; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, Jilin, China.
  • Pan Y; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Yuan B; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Wang Y; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Zhou Q; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Meng X; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Jing J; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Lin J; Tiantan Hospital, China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Wang A; Neurology, China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Zhang S; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Hong Z; Neurology, China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Yang Y; Department of Neurology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
  • Xiong Y; Department of Neurology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
  • Li Z; Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, Jilin, China.
  • Wang Y; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Zhao X; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Wang Y; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Stroke Vasc Neurol ; 2024 Jun 14.
Article em En | MEDLINE | ID: mdl-38789134
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Stroke Vasc Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Stroke Vasc Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China
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