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临床试验/NCT03772847
NCT03772847已完成4 期

Ginkgolide With Intravenous Alteplase Thrombolysis in Acute Ischemic Stroke Neurological Improving Trial

Second Affiliated Hospital, School of Medicine, Zhejiang University1 个研究点 分布在 1 个国家目标入组 1,189 人开始时间: 2018年7月31日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
1,189
试验地点
1
主要终点
proportion of patients with a 90-day modified Rankin Scale (mRS) score below 2

研究概览

简要总结

Previous clinical studies have confirmed that revascularization or recanalization rate after intravenous thrombolysis is closely related to the formation of thrombus, which also results in poor neurological function after thrombolysis. Platelet activating factor (PAF) strong platelet aggregation may be involved in thrombosis. Formation process. The main components of Ginkgolide injection (Ginkgo) are ginkgolide, ginkgolides A, ginkgolides B and ginkgolides C. Ginkgo biloba lactone can antagonize PAF and has strong anti-platelet aggregation. . Therefore, it can be speculated that ginkgolides injection combined with alteplase intravenous thrombolysis may improve the recanalization rate after thrombolysis and reduce the reocclusion rate.

In addition, clinical studies have also found that ginkgolide injection has a good auxiliary effect on hypertensive intracerebral hemorrhage, which can regulate inflammatory factors such as IL-6, TNF-α and high-sensitivity C-reactive protein (CRP) in patients. Recovery of neurological function in patients. It is well known that TNF-α, IL-β, IL-1, IL-6, IFN-γ, etc. are all inflammatory factors associated with reperfusion injury. Therefore, we speculate that ginkgolides injection may also regulate inflammatory factors associated with reperfusion injury, such as IL-6, TNF-α, thereby reducing reperfusion injury, thereby improving patient prognosis.

The aim of this study was to determine the clinical efficacy of ginkgolides injection combined with alteplase in the treatment of acute ischemic stroke, and to improve the prognosis of patients with thrombolysis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age over 18 years old, clinically diagnosed as acute ischemic stroke;
  • in accordance with the indications for intravenous thrombolysis;
  • The patient or family member signs an informed consent form.

排除标准

  • Patients with transient ischemic attack;
  • Imaging examination of patients with cerebral hemorrhage
  • patients with cerebral arteritis
  • ALT, AST ≥ 3 times the upper limit of normal value, Cr ≥ 1.5 times the upper limit of normal value
  • There is a tendency to bleed, and severe bleeding has occurred within 3 months
  • Patients with ginkgo drugs, alcohol, glycerol allergies or allergies
  • Patients with pregnancy plans, pregnancy and breastfeeding
  • Patients who participated in other drug clinical studies in the past month
  • Patients considered by the investigator to be unfit to participate in the clinical study (eg, mental, abnormal, etc.)

研究组 & 干预措施

ginkgolide group

Experimental

ginkgolide plus alteplase

干预措施: ginkgolide (Drug)

结局指标

主要结局

proportion of patients with a 90-day modified Rankin Scale (mRS) score below 2

时间窗: 90 days

mRS 0-6, higher indicate worse outcome

次要结局

  • National Institute of Health Stroke Scale(NIHSS) scores between the two groups at baseline, 24 hours, 7 days, and 14 days(14 days)
  • incidence of compound events (include cerebrovascular events,myocardial infarction, angina pectoris, and systemic embolism)(1 year)
  • recurrence rate of cerebrovascular disease in 1-month and 3-month follow-up(3 months)

研究者

发起方
Second Affiliated Hospital, School of Medicine, Zhejiang University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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