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临床试验/NCT04958512
NCT04958512已完成不适用

Clinical Study of Yangxue Qingnao Pill in the Treatment of Mild Vascular Cognitive Impairment Without Dementia (VCIND)

Peking University Third Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2017年8月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Montreal Cognitive Assessment Scale (MoCA)

研究概览

简要总结

In this study, the effectiveness of vascular cognitive impairment was compared among the three groups, namely, the xidezhen group, the Yangxue Qingnao pill group and the placebo group

详细描述

The risk factors of various cerebrovascular diseases (atherosclerosis, stroke, hypertension, coronary heart disease, atrial fibrillation, dyslipidemia, diabetes mellitus) are both risk factors of Alzheimer's disease and one of the many causes of vascular dementia. There are many manifestations of mental retardation caused by cerebrovascular diseases. The most prominent aspect is cognitive and behavioral impairment, which is characterized by mental retardation, forgetfulness, misunderstanding and poor calculation ability. Yangxue Qingnao pill (z20063808:) is produced by Tianshili Pharmaceutical Group Co., Ltd, And then improve the ability of learning and memory. Some clinical application results show that the drug can significantly improve the cognitive and behavioral ability of patients with ischemic stroke, improve the cognitive function of patients with mild Alzheimer's disease, and improve the quality of life. Therefore, this study mainly compared the effectiveness of treatment of vascular cognitive impairment in three groups, namely, the xidezhen group, the yangxueqingnaowan group and the placebo group.

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
Double (Participant, Investigator)

入排标准

年龄范围
50 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Over 50 years old, under 85 years old, male and female, including 50 and 85 years old;
  • The patients agreed to participate in the trial and signed the informed consent.
  • The diagnostic criteria for vascular cognitive impairment without dementia are as follows:
  • There are risk factors of cerebrovascular disease or the existence of cerebrovascular disease;
  • The development of cognitive impairment was fluctuating;
  • Mild memory impairment or retention;
  • There is a causal relationship between cerebrovascular disease and cognitive impairment, and other diseases are excluded;
  • The activities of daily living remained normal;
  • According to the diagnostic criteria of mild cognitive impairment (MCI) developed by Xiao Shifu, the subjects' MMSE score was less than or equal to 26

排除标准

  • The researchers considered that it was not suitable to be included in the study;
  • Known liver diseases of clinical significance, which may hinder patients from completing the test, and / or total bilirubin, aspartate aminotransferase, alanine aminotransferase and alkaline phosphatase are 1.5 times higher than the upper limit of normal value;
  • The patients with known clinically significant kidney disease may be prevented from completing the test, and / or the serum creatinine is higher than the normal range in the laboratory, and / or the blood urea nitrogen is 1.5 times higher than the normal range;
  • He had a history of acute cerebrovascular disease within 3 months;
  • At present, there is active epilepsy;
  • History of mental illness;
  • Peptic ulcer and gastrointestinal bleeding;
  • Any of the tested drugs was taken within 28 days before medication, which may cause cognitive changes and important organ damage.
  • Accompanied by unstable blood system and immune system diseases, is not in clinical remission.
  • Malignant tumor or intracranial tumor is known;
  • Those who had surgery within three months or had a history of trauma.
  • There are other advanced, serious or unstable diseases, which affect the evaluation of its efficacy and safety;

研究组 & 干预措施

blank control group

Other

干预措施: blank control group (Other)

treatment group(Yangxue Qingnao pill)

Experimental

干预措施: Yangxue Qingnao pill (Drug)

control group(hidezhen)

Active Comparator

干预措施: Hydergotoxine mesylate tablets (Drug)

结局指标

主要结局

Montreal Cognitive Assessment Scale (MoCA)

时间窗: at 6th month

Level of cognition,ranging from 0-30 points, the higher score means better outcome

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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