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
| Type | Name | Description |
|---|---|---|
| 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 |
| DRUG | 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. |
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.