Clinical Trials Directory

Trials / Completed

CompletedNCT04958512

Treatment of Mild Vascular Cognitive Impairment With Yangxue Qingnao Pill

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Peking University Third Hospital · Academic / Other
Sex
All
Age
50 Years – 85 Years
Healthy volunteers
Not accepted

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGYangxue Qingnao pillThe treatment group (20 cases) was treated with Yangxue Qingnao pill (2.5g / time, 3 times / day, orally for 6 months
DRUGHydergotoxine mesylate tabletsThe control group (n = 20) was treated with hidezhen 3 mg per day before meals for 6 months
OTHERblank control groupThere were 20 cases in the blank control group.Outpatient consultation at any time was prescribed.

Timeline

Start date
2017-08-30
Primary completion
2018-01-31
Completion
2018-03-31
First posted
2021-07-12
Last updated
2021-07-12

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04958512. Inclusion in this directory is not an endorsement.