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临床试验/NCT04509323
NCT04509323Unknown4 期

A Randomized, Controlled, Single-center Clinical Study of Huperzine A in the Treatment of Brain Injury in Patients With Hypertensive Cerebral Hemorrhage

Jiangsu Famous Medical Technology Co., Ltd.1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2020年8月3日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
20
试验地点
1
主要终点
Extension of Glasgow Outcome Scale(GOSE) Scores at 90 days of treatment

研究概览

简要总结

  1. To evaluate the effectiveness of Huperzine A injection in the treatment of brain injury in patients with hypertensive cerebral hemorrhage;
  2. To evaluate the safety of Huperzine A injection in the treatment of brain injury in patients with hypertensive cerebral hemorrhage。

详细描述

A randomized, controlled, single-center, exploratory clinical research method was used. In the treatment plan, the experimental group used basic treatment + Huperzine A, and the control group only used basic treatment, with a total of 20 cases. To evaluate the effectiveness and safety of Huperzine A injection in the treatment of brain injury in patients with hypertensive cerebral hemorrhage.

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged from 18 to 75 years old(including 18 and 75 years old), males or females;
  • First onset, clinical diagnosis of hypertensive intracerebral hemorrhage, and CT confirmed that the amount of hemorrhage is between 15ml-50ml, the bleeding site is the basal ganglia, the bleeding has not penetrated into the lateral ventricle, and non-surgical patients;
  • Those with obvious neurological dysfunction after the onset, 5≤GCS≤15 or NIHSS≥6;
  • Admission within 72 hours after the onset of the disease, and no significant enlargement of the hematoma within 24 hours after admission (hematoma enlargement ≤ 5ml);
  • The patient/family knows and signs the informed consent form voluntarily.

排除标准

  • Cerebral hemorrhage caused by cerebral aneurysm, brain tumor, brain trauma, cerebral parasitic disease, cerebrovascular malformation, abnormal blood vessel network at the base of the brain, cerebral arteritis, blood disease, metabolic disorder and other diseases confirmed by examination;
  • Patients with enlarged hematoma found within 24 hours after admission (the volume of enlarged hematoma> 5ml);
  • Patients with simple transient ischemic attack, lacunar infarction, subarachnoid hemorrhage and ischemic cerebral infarction;
  • Patients who use anticoagulant drugs for a long time;
  • Patients with platelet count <100,000, INR>1.4 at admission and abnormal blood coagulation function;
  • The measured value of homocysteine at admission is higher than 15μmol/L;
  • Patients who need surgical treatment (including ventricular drainage);
  • Patients with severe primary diseases such as cardiovascular, liver (ALT or AST>1.5 times the upper limit of normal), kidneys (BUN>1.5 times the upper limit of normal and Cr>upper limit of normal), endocrine system and hematopoietic system;
  • Those who are allergic to protein and test drugs;
  • People who are dependent on drugs or alcohol;
  • Intended pregnancy or women of childbearing age with positive pregnancy test and lactating women;
  • Participated in other clinical trials within the past 3 months;
  • Patients considered by the investigator to be inappropriate to participate in clinical trials.

研究组 & 干预措施

Experimental:Huperzine A for Injection+Basic treatment

Experimental

Huperzine A for Injection: Dissolve each bottle with 2ml sterile water for injection and inject into muscle, the course of treatment is 14 days; Basic treatment:Control blood pressure; prevent continued bleeding; prevent and treat gastrointestinal bleeding; decide whether to perform dehydration treatment according to the condition to reduce cerebral edema; prevent infection, prevent various complications, etc.; routine rehabilitation training.

干预措施: Huperzine A for Injection (Drug)

结局指标

主要结局

Extension of Glasgow Outcome Scale(GOSE) Scores at 90 days of treatment

时间窗: At the 90-day

At the 90-day follow-up of patients, the extended Glasgow Outcome Scale (GOSE) was used to assess and judge the difference in consciousness after stroke between the two groups. The scores of minimum values is 1, the maximum values is 8, whether higher scores mean a better outcome.

次要结局

  • Extension of Glasgow Outcome Scale(GOSE) Scores at 30 days of treatment(At the 30-day)
  • Scores of Modified Rankin Scale(mRS) at 30 days of treatment(At the 30-day)
  • Scores of Modified Rankin Scale(mRS) at 14 days of treatment(At the 14-day)
  • Scores of National Institute of Health stroke scale(NIHSS) at 14 days of treatment(At the 14-day)
  • Scores of National Institute of Health stroke scale(NIHSS) at 30 days of treatment(At the 30-day)
  • Complication rate(At the 90-day)
  • Scores of Modified Rankin Scale(mRS) at 90 days of treatment(At the 90-day)
  • Scores of National Institute of Health stroke scale(NIHSS) at 90 days of treatment(At the 90-day)
  • Scores of the Barthelindex of ADL at 30 days of treatment(At the 30-day)
  • Scores of the Barthelindex of ADL at 14 days of treatment(At the 14-day)
  • Scores of the Barthelindex of ADL at 90 days of treatment(At the 90-day)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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