Songling Xuemaikang Capsules for Cerebral Small Vessel Disease

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age55-75
SponsorDongzhimen Hospital, Beijing

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.);

Trial design

Design model

Parallel

Treatments tested in this trial

  • 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)

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Test groupExperimental treatment 1 intervention
Group B: Control groupPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

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

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

Time frame
1 year

Secondary outcomes

1

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

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

Time frame
1 year
2

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

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

Time frame
1 year
3

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

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

Time frame
1 year
4

Change from baseline in Pittsburgh Sleep Quality Index (PSQI) at 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.

Time frame
1 year

Other outcomes

1

Numbers in new vascular events from baseline to 1 year

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

Time frame
1 year
2

Numbers in all-cause hospitalization from baseline to 1 year

Numbers in all-cause hospitalization

Time frame
1 year

Sponsors and contacts

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