Treatment of Mild Vascular Cognitive Impairment With Yangxue Qingnao Pill

Cerebrovascular Diseases Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04958512
• Other study ID #: M2017154
• Status: Completed
• Phase: N/A
• Start date: August 30, 2017
• Est. completion date: March 31, 2018

Study information

• Verified date: June 2021
• Source: Peking University Third Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: March 31, 2018
• Est. primary completion date: January 31, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 50 Years to 85 Years

Eligibility

Inclusion Criteria:

1. Over 50 years old, under 85 years old, male and female, including 50 and 85 years old;

2. The patients agreed to participate in the trial and signed the informed consent.

3. The diagnostic criteria for vascular cognitive impairment without dementia are as

follows:

1. There are risk factors of cerebrovascular disease or the existence of cerebrovascular disease;

2. The development of cognitive impairment was fluctuating;

3. Mild memory impairment or retention;

4. There is a causal relationship between cerebrovascular disease and cognitive impairment, and other diseases are excluded;

5. The activities of daily living remained normal;

6. 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

Exclusion Criteria:

1. The researchers considered that it was not suitable to be included in the study;

2. 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;

3. 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;

4. He had a history of acute cerebrovascular disease within 3 months;

5. At present, there is active epilepsy;

6. History of mental illness;

7. Peptic ulcer and gastrointestinal bleeding;

8. Any of the tested drugs was taken within 28 days before medication, which may cause cognitive changes and important organ damage.

9. Accompanied by unstable blood system and immune system diseases, is not in clinical remission.

10. Malignant tumor or intracranial tumor is known;

11. Those who had surgery within three months or had a history of trauma.

12. There are other advanced, serious or unstable diseases, which affect the evaluation of its efficacy and safety;

Related Conditions & MeSH terms

• Cerebrovascular Diseases
• Cerebrovascular Disorders
• Cognitive Dysfunction

Intervention

Drug:
• Yangxue Qingnao pill
The treatment group (20 cases) was treated with Yangxue Qingnao pill (2.5g / time, 3 times / day, orally for 6 months
• Hydergotoxine mesylate tablets
The control group (n = 20) was treated with hidezhen 3 mg per day before meals for 6 months

Other:
• blank control group
There were 20 cases in the blank control group.Outpatient consultation at any time was prescribed.

Locations

Country	Name	City	State
China	Peking University Third Hospital	Beijing	Beijing

Sponsors (2)

Lead Sponsor	Collaborator
Peking University Third Hospital	Beijing Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Montreal Cognitive Assessment Scale (MoCA)	Level of cognition,ranging from 0-30 points, the higher score means better outcome	at 6th month