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临床试验/EUCTR2018-002176-41-IT
EUCTR2018-002176-41-IT进行中(未招募)1 期

Prevention of Stroke in Intracerebral Haemorrhage Survivors with Atrial Fibrillation (PRESTIGE-AF) - PRESTIGE-AF

Imperial College of Science, Technology and Medicine0 个研究点目标入组 654 人开始时间: 2021年1月21日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
654

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Age = 18 years
  • - Written informed consent
  • - Recent history of a non-traumatic spontaneous ICH during the 6 months before enrolment
  • - Documented evidence of AF (paroxysmal, persistent or permanent)
  • - CHA2DS2-VASc score=2 for male, and CHA2DS2-VASc score= 3 for female patients
  • - Availability of brain imaging following the index Intracerebral Haemorrhage (ICH)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 100
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 554

排除标准

  • 1. Patient lacks capacity to consent
  • 2. Fully dependent (defined as a modified Rankin Scale score of over 4)
  • 3. Women who are pregnant, breastfeeding, or plan to become pregnant during the Study period
  • 4. Women of childbearing potential (WOCBP) who are unable or unwilling to take measures for effective contraception
  • 5. ICH occurring within the last 14 days before enrolment
  • 6. ICH occurring longer than 6 months before enrolment
  • 7. ICH resulting from trauma or vascular malformation
  • 8. Another indication for long-term anticoagulation
  • 9. Contraindication for long-term anticoagulant therapy with DOACs (other than ICH)
  • 10. Absolute need for antiplatelet therapy at enrolment
  • 11. Presence of a left atrial appendage occlusion device (LAAO) or plan to implant an LAAO
  • 12. Presence of any medical, psychological, or psychiatric condition which in the opinion of the Principal or Co-Investigator would cause participation in the Study to be unwise
  • 13. Participation in any clinical study with an Investigational Medicinal Product within the past 30 days (observationalstudies are permitted)

研究者

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Prevention of Stroke in Survivors of Brain Bleeding... | 临床试验