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临床试验/ITMCTR2024000033
ITMCTR2024000033已完成1 期

Efficacy and Safety of Angong Niuhuang Pill in Patients With Acute Ischemic Stroke

Affiliated Hangzhou First People's Hospital, Xihu University School of Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方

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 100(—)
性别
All

入选标准

  • 1.Being 18 years of age or older; 2.Having experienced an acute ischemic stroke; 3.Being within 24 hours of stroke onset or last-seen well; 4.Having a National Institutes of Health Stroke Scale (NIHSS) score of at least 6 before entering the trial; 5.Undergoing multimodal imaging assessment where CT artery (CTA) confirmed that the stroke was caused by occlusion of a large vessel in the anterior circulation; 6.The patients or their legal representatives providing signed informed consent.

排除标准

  • 1.NCCT suggests intracranial hemorrhage;
  • 2.Active bleeding or a significant bleeding tendency;
  • 3.Patients with renal failure, serum creatinine =264umol/L;
  • 4.pre-existing mRS=2;
  • 5.previous allergy to contrast media; Allergic to known ingredients of Angong Niuhuang pills;
  • 6.Multiple organ failure, can not tolerate surgery
  • 7.The expected survival time of other diseases (such as malignant tumors) is less than 3 months

研究者

发起方
Affiliated Hangzhou First People's Hospital, Xihu University School of Medicine

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