跳至主要内容
临床试验/ISRCTN18274006
ISRCTN18274006进行中(未招募)未知

Rates, Risks and Routes to Reduce Vascular Dementia

Academic and Clinical Central Office for Research and Development (ACCORD)0 个研究点目标入组 2,000 人开始时间: 2019年7月29日最近更新:
适应症

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
2,000

研究概览

简要总结

2024 Preprint results in https://doi.org/10.1101/2024.04.30.24306637 (added 21/06/2024)

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • Current inclusion criteria as of 17/06/2020:
  • 1. Patients aged 18 and over
  • 2. No upper age limit
  • 3. No severity limit
  • 4. Ischaemic or spontaneous haemorrhagic (non-traumatic, non-subarachnoid haemorrhage, non-AVM) stroke and transient ischaemic attack (TIA)
  • 5. Expected to survive at least 12 weeks
  • DTI substudy only
  • 1. Estimated life expectancy >= 1 year
  • 2. No contraindications to MRI
  • 3. Patients with capacity to consent at baseline
  • COVID-19 substudy: expected to survive 12 weeks is not an inclusion criterion.
  • Previous inclusion criteria:
  • 1. Patients aged 18 and over
  • 2. No upper age limit
  • 3. No severity limit
  • 4. Ischaemic or spontaneous haemorrhagic (non-traumatic, non-subarachnoid haemorrhage, non-AVM) stroke and transient ischaemic attack (TIA)
  • 5. Expected to survive at least 12 weeks

排除标准

  • 1. Inclusion criteria not met
  • 2. Aneurysmal, traumatic or AVM-associated haemorrhage or subarachnoid haemorrhage
  • 3. Stroke mimics such as brain tumours
  • 4. Prior diagnosis of cognitive impairment or dementia is NOT an exclusion criteria

研究者

发起方
Academic and Clinical Central Office for Research and Development (ACCORD)

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