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临床试验/EUCTR2018-000790-79-NL
EUCTR2018-000790-79-NL进行中(未招募)1 期

IMPROVING OUTCOME IN SUBARACHNOID HEMORRHAGE WITH NADROPARINE - ISCHEMIA

Academic Medical Centre Amsterdam0 个研究点目标入组 100 人开始时间: 2021年6月8日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
100

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

  • SAH confirmed by CT or lumbar puncture with the causative aneurysm confirmed by CT-A and/or DSA
  • Coiling of the causative aneurysm within 72 hours of initial SAH
  • Informed consent within 24 hours after coiling
  • Adult age (=18 years)
  • 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 60
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 40

排除标准

  • Stent-assisted coiling
  • Contra-indications for LMWH: History of heparin-induced thrombocytopenia, Active bleeding, Known hemorrhagic diathesis due to coagulation disorders (with the exception of dis-seminated intravascular coagulation), Severe hypertension: uncontrolled hypertension with a MAP > 135mmHg, History of hypertensive or diabetic retinopathy, Active infectious endocarditis, Severe renal impairment (creatinine clearance <30 mL / min)
  • No proficiency of Dutch or English language
  • No informed consent

研究者

发起方
Academic Medical Centre Amsterdam

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