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临床试验/NL-OMON51205
NL-OMON51205尚未招募2 期

Complement Inhibition: Attacking Overshooting inflammation @fter Subarachnoid Hemorrhage (CIAO@SAH trial) - CIAO@SAH

Haaglanden Medisch Centrum0 个研究点目标入组 128 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
入组人数
128

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

年龄范围
18 至 99(—)

入选标准

  • - Confirmed diagnosis of aneurysmal subarachnoid hemorrhage on CT-scan
  • - Age >= 18 years on admission
  • - WFNS grade 1-5

排除标准

  • - Subarachnoid hemorrhage deemed most likely to *peri mesencephalic* origin
  • after consideration of history, clinical examination and radiological findings
  • (including angiographic imaging);
  • - Subarachnoid hemorrhage deemed most likely of post-traumatic origin after
  • consideration of history, clinical examination and radiological findings
  • (including angiographic imaging);
  • - Participation in another clinical therapeutic study;
  • - Patients with definite infaust prognosis on arrival and/or expected death
  • within 24 hours of admission;
  • - Patients with a known hereditary complement deficiency (including hereditary
  • angioedema);
  • - Patients with a history of sensibility to blood products or C1-inhibitor;
  • - Patients with a history of thrombosis (when known at time of inclusion);
  • - Pregnant woman.

研究者

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