CTIS2024-511679-14-00进行中(未招募)1 期
Improving outcome in subarachnoid hemorrhage with nadroparin
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 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
- 年龄范围
- 18 至 65+(—)
- 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 before the first scheduled administration of the study medicine, Adult age (=18 years)
排除标准
- •Stent-assisted coiling, Use of anticoagulant or dual antiplatelet medication post-coiling for other reasons, Incomplete aneurysm occlusion/partial coiling, Intraparenchymal hemorrhage, Pregnancy, Contra-indications for LMWH: oPrevious history of history of heparin-induced thrombocytopenia o(Suspicion of) active arterial or venous bleeding oPrevious history of hemorrhagic diathesis due to coagulation disorders (with the ex-ception of disseminated intravascular coagulation) oSevere hypertension: uncontrolled hypertension with a MAP > 135mmHg oPrevious history of hypertensive or diabetic retinopathy oPrevious history of active infectious endocarditis oSevere renal impairment (creatinine clearance <30 mL / min), No proficiency of Dutch or English language, Proven and active COVID-19 infection
研究者
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