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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)
Lead sponsor
Asset
Hydergotoxine mesylate
Listed sites
1
Recruiting sites
-
Enrollment
60
actual
Study population
Vascular cognitive impairment / dementia
Key I/E criterion
•MMSE ≤26
Primary endpoint
•Montreal Cognitive Assessment (MoCA)
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Drug assets
Study populations
Who this study enrolls
Eligibility
Who can enroll
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;
Endpoints (1)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Global cognition
1 endpointMontreal Cognitive Assessment Scale (MoCA)
Time frame:at 6th month
Montreal Cognitive Assessment (MoCA)
descriptive
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 21, 2026 snapshot.