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
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