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CompletedPhase NA

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)

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

Org study IDM2017154
NCT IDNCT04958512

Timeline

Milestones

Study start2017-08-30actual
Primary completion2018-01-31actual
Study completion2018-03-31actual
Study first posted2021-07-12actual
Last update posted2021-07-12actual

Assets

Drug assets

Study populations

Who this study enrolls

Vascular cognitive impairment / dementia

Eligibility

Who can enroll

Minimum age50 Years
Maximum age85 Years
SexAll
Healthy volunteersNot accepted

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 endpoint
Primary/protocol endpoint

Montreal Cognitive Assessment Scale (MoCA)

Time frame:at 6th month

Montreal Cognitive Assessment (MoCA)

descriptive

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 21, 2026
Endpoint classificationDelfa ADRD endpoint taxonomy
Results tableno registry results posted yet

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.