NL-OMON22901尚未招募不适用
Complement C5 Antibodies for decreasing brain injury after aneurysmal Subarachnoid Hemorrhage: safety and proof-of-concept
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1) Confirmed aneurysmal SAH
- •2) Admission to the UMCU within 12 hours after ictus
排除标准
- •1) Life expectancy < 10 days;
- •2) Pregnant or breast-feeding women;
- •3) Participation in another clinical therapeutic study;
- •4) History of splenectomy or asplenia (potentially increased risk of meningococcal infection);
- •5) Hematologic malignancy;
- •6) Patients receiving chemotherapy;
- •7) Patients who will undergo or underwent an organ transplantation;
- •8) Patients with myasthenia gravis, glucose-6-phosphate dehydrogenase (G6PD) deficiency, or tuberculosis;
- •9) Patients who are or will be treated by plasmapheresis or hemodialysis;
- •10) Patient with a creatinine clearance of <30 or serum creatinine levels of >169 µmol/l
- •11) Patients with a known hereditary complement deficiency;
- •12) Patients allergic to eculizumab, proteins derived from mouse products or other monoclonal antibodies;
- •13) Patients allergic to (prophylactic) antibiotic treatment for Neisseria meningitidis (quinolones or ceftriaxone (therapeutic));
- •14) If on admission, it is likely that the aneurysm can only be treated with extracranial-intracranial bypass surgery;
- •15) If based on head imaging, it will be unlikely that CSF can be obtained 48-72 hours after ictus;
- •16) Patients with an ongoing infection on admission which is not appropriately treated;
- •17) Patients who were treated >4 times with antibiotics during the last year;
- •18) Patients on immunosuppressive therapy.
研究者
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