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
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