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NCT Number: NCT07271732

Songling Xuemaikang Capsules for Cerebral Small Vessel Disease

Cerebral small vessel disease (CSVD) is a common age-related microvascular disease related to the slow accumulation of damage to small arteries, veins, and capillaries. Hypertension is a risk factor for cerebrovascular disease, and its damage to the vascular endothelium is one of the key contributing factors to the pathogenesis of CSVD. CSVD has an insidious onset, and patients may exhibit no clinical symptoms in the early stage. Common clinical manifestations of chronic CSVD include vascular dementia, depression, gait disturbance, and abnormalities in swallowing and urinary functions. There is currently no specific treatment for CSVD.

Existing studies have shown that Songling Xuemaikang capsule (SXC) combined with antihypertensive drugs exerted significant effects on systolic blood pressure (SBP), diastolic blood pressure (DBP), 24-hour SBP, and 24-hour DBP, while also improving symptoms of hypertension. Animal experiments have demonstrated that SXC can reduce apoptosis and alleviate cerebral ischemia-reperfusion injury, exerting neuroprotective effects. Additionally, a previously completed multicenter, randomized, double-blind, non-inferiority-designed clinical trial by the team, conducted in patients with primary hypertension, showed that SXC were non-inferior to losartan potassium in reducing diastolic blood pressure. Therefore, exploring the therapeutic potential of SXC in CSVD is highly necessary.

This project is a randomized, double-blind, placebo-controlled multicenter clinical study to investigate the clinical efficacy and safety of SXC in the treatment of hypertension with CSVD. A total of 90 subjects who met the subject screening criteria are planned to be enrolled, with 45 patients in the test group and 45 patients in the placebo group.

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Key information

Age range

55 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 55-75 years (both inclusive);
  • MRI has moderate to (1) severe white matter lesions (deep Fazekas score > 1 or paraventricular Fazekas score > 2 or modified Fazekas score > 1), or (2) mild white matter hyperintensity (deep Fazekas score = 1 or paraventricular Fazekas score = 2 or modified Fazekas score = 1) combined with more than 1 lacunar infarction;
  • History of essential hypertension; Hypertension is defined as SBP consistently greater than 140 mmHg and/or DBP consistently greater than 90 mmHg, or those requiring clinical antihypertensive treatment.
  • Meeting the diagnostic criteria for hyperactivity of liver yang pattern; Hyperactivity of liver yang pattern is defined as having at least three of the following six symptoms: headache, dizziness or vertigo, irritability, flushed face, red eyes, and yellow tongue coating.
  • Functional independence in daily living (Modified Rankin Scale ≤2);
  • Voluntary participation in the study and be willing to sign the Informed Consent Form.

Exclusion criteria

  • Patients with acute ischemic stroke or acute intracranial hemorrhage (e.g., epidural hematoma, subdural hematoma, subarachnoid hemorrhage, intracerebral hemorrhage, etc.) or a history of cerebral infarction (non-lacunar) or intracranial hemorrhage within the past 3 months;
  • Symptomatic stenosis of the middle cerebral artery and/or internal carotid artery (stenosis rate ≥50%), or asymptomatic stenosis of the middle cerebral artery and/or internal carotid artery (stenosis rate ≥70%);
  • Untreated cerebrovascular malformations or intracranial aneurysms (diameter >3 mm);
  • Significant non-vascular white matter lesions (e.g., multiple sclerosis, adult-onset leukoencephalopathy, metabolic encephalopathy, etc.);
  • Patients with a history of cognitive impairment due to other causes (e.g., normal pressure hydrocephalus, Alzheimer's disease, Parkinson's disease, multiple sclerosis, encephalitis, etc.);
  • A history of intracranial or intramedullary surgery within the past year;
  • Severe hepatic, renal, or cardiac insufficiency (ALT or AST >2 times the upper limit of normal, or serum creatinine >1.5 times the upper limit of normal, or New York Heart Association [NYHA] functional class III or IV);
  • Severe three-vessel coronary artery disease as shown by coronary computed tomography angiography or coronary angiography within 90 days or suffering from frequent angina;
  • Refractory hyperglycemia uncontrolled by medication (fasting blood glucose >10 mmol/L, or HbA1c >8.0%);
  • Patients with severe diseases such as cancer and a life expectancy of less than 2 years;
  • Patients with psychiatric disorders that affect study medication administration and evaluation;
  • Previous allergy or intolerance to Songling Xuemaikang Capsules;
  • Contraindications to MRI examination (e.g., claustrophobia, presence of an implantable pacemaker, etc.);
  • Patients unable to comply with follow-up examinations or other study procedures due to residential location or other reasons;
  • Participation in other clinical trial projects.

Treatment and study plan

Songling Xuemaikang Capsule

Drug

3 capsules/time, tid, p.o Duration of Treatment: 1 year (12 months)

Songling Xuemaikang Capsule Placebo

Drug

3 capsules/time, tid, p.o Duration of Treatment: 1 year (12 months)

Primary outcomes

  1. Changes in the volume of white matter hyperintensities at 1 year.

    Time frame: 1 year

    Measure changes in the volume of white matter hyperintensities on brain MRI

Secondary outcomes

  1. Change from baseline in Mini-Mental State Examination (MMSE) at 1 year;

    Time frame: 1 year

    Change from baseline in Mini-Mental State Examination (MMSE). Score range is 0-30. Higher score means good cognition.

  2. Change from baseline in Hamilton Anxiety Scale (HAMA) at 1 year;

    Time frame: 1 year

    Change from baseline in Hamilton Anxiety Scale (HAMA).Score range is 0-56. Higher score means a more severe state of anxiety.

  3. Change from baseline in Hamilton Depression Scale (HAMD) at 1 year;

    Time frame: 1 year

    Change from baseline in Hamilton Depression Scale (HAMD). Score range is 0-76. Higher score means a more severe state of anxiety.

  4. Change from baseline in Pittsburgh Sleep Quality Index (PSQI) at 1 year;

    Time frame: 1 year

    Change from baseline in Pittsburgh Sleep Quality Index (PSQI) at 1 year. Score range is 0-21. Higher score means worse sleep quality.

  5. Change from baseline in Barthel Index (BI) at 1 year;

    Time frame: 1 year

    Change from baseline in Barthel Index (BI). Score range is 0-100. Higher score means good physical activities of daily living.

  6. Feasibility of recruitment and retention

    Time frame: 1 year

    The feasibility is defined as >95% of randomized patients retained at 1 year

  7. Change from baseline in the symptom of hyperactivity of liver yang pattern at 1 year;

    Time frame: 1 year

    Change from baseline in the symptom of hyperactivity of liver yang pattern, which are headache, dizziness or vertigo, irritability, flushed face, red eyes, and yellow tongue coating. The study plans to analyze whether there are statistically significant differences in the incidence of the above six symptoms before and after treatment. On the other hand, for headache, dizziness or vertigo, irritability, if they do not resolve at follow-up time points, patient-reported outcomes (PROs) will be used to record the degree of change in patients' symptoms from baseline (expressed as a percentage, with >100% indicating symptom worsening and <100% indicating symptom relief), and statistical analysis will be carried out. For flushed face, red eyes, and yellow tongue coating, binary analysis will be performed based solely on their presence or absence.

  8. Change from baseline in the mean 24h systolic blood pressure at 1 year;

    Time frame: 1 year

    Change from baseline in the mean 24h systolic blood pressure

  9. Change from baseline in the mean 24h diastolic blood pressure at 1 year;

    Time frame: 1 year

    Change from baseline in the mean 24h diastolic blood pressure

  10. Change from baseline in the mean daytime systolic blood pressure at 1 year;

    Time frame: 1 year

    Change from baseline in the mean daytime systolic blood pressure

  11. Change from baseline in the mean daytime diastolic blood pressure at 1 year;

    Time frame: 1 year

    Change from baseline in the mean daytime diastolic blood pressure

  12. Change from baseline in the mean nighttime systolic blood pressure at 1 year

    Time frame: 1 year

    Change from baseline in the mean nighttime systolic blood pressure

  13. Change from baseline in the mean nighttime diastolic blood pressure at 1 year

    Time frame: 1 year

    Change from baseline in the mean nighttime diastolic blood pressure

  14. Change from baseline in the mean 24h pulse pressure at 1year

    Time frame: 1 year

    Change from baseline in the mean 24h pulse pressure

  15. Change from baseline in the blood pressure load at 1 year

    Time frame: 1 year

    Change from baseline in the blood pressure load

  16. Change from baseline in the official systolic blood pressure at 1 year

    Time frame: 1 year

    Change from baseline in the official systolic blood pressure

  17. Change from baseline in the official diastolic blood pressure at 1 year

    Time frame: 1 year

    Change from baseline in the official diastolic blood pressure

  18. Change from baseline in the official pulse pressure at 1year

    Time frame: 1 year

    Change from baseline in the official pulse pressure

  19. Change from baseline in the official blood pressure compliance rate at 1 year

    Time frame: 1 year

    Change from baseline in the official blood pressure compliance rate

Other outcomes

  1. Numbers in new vascular events from baseline to 1 year

    Time frame: 1 year

    New vascular events include ischemic stroke, TIA, cerebral hemorrhage, MI, pulmonary embolism, thrombosis, peripheral arterial occlusion

  2. Numbers in all-cause hospitalization from baseline to 1 year

    Time frame: 1 year

    Numbers in all-cause hospitalization

Study contacts

Contact information is provided by the study sponsor or research team.

Xinxing Lai, PhD

CONTACT

[email protected]

+86-15901111280

Sponsors and collaborators

Lead sponsor

Dongzhimen Hospital, Beijing

Other

Registry information

Official study title

Songling Xuemaikang Capsules for Cerebral Small Vessel Disease: A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Study

Acronym: SXC-CSVD

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 9, 2025
Registry last updated
Dec 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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