Dongzhimen Hospital, Beijing University of Chinese Medicine
Beijing, Beijing Municipality, 100700, China
Location contact
Xinxing Lai, PhD
CONTACT
Yupeng WEI
CONTACT
NCT Number: NCT07271732
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.
Trial opening soon.
Get Notified55 year–75 year
All sexes
Interventional
Not applicable
Beijing, Beijing Municipality, 100700, China
Xinxing Lai, PhD
CONTACT
Yupeng WEI
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
3 capsules/time, tid, p.o Duration of Treatment: 1 year (12 months)
3 capsules/time, tid, p.o Duration of Treatment: 1 year (12 months)
Time frame: 1 year
Measure changes in the volume of white matter hyperintensities on brain MRI
Time frame: 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
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
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
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
Change from baseline in Barthel Index (BI). Score range is 0-100. Higher score means good physical activities of daily living.
Time frame: 1 year
The feasibility is defined as >95% of randomized patients retained 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.
Time frame: 1 year
Change from baseline in the mean 24h systolic blood pressure
Time frame: 1 year
Change from baseline in the mean 24h diastolic blood pressure
Time frame: 1 year
Change from baseline in the mean daytime systolic blood pressure
Time frame: 1 year
Change from baseline in the mean daytime diastolic blood pressure
Time frame: 1 year
Change from baseline in the mean nighttime systolic blood pressure
Time frame: 1 year
Change from baseline in the mean nighttime diastolic blood pressure
Time frame: 1 year
Change from baseline in the mean 24h pulse pressure
Time frame: 1 year
Change from baseline in the blood pressure load
Time frame: 1 year
Change from baseline in the official systolic blood pressure
Time frame: 1 year
Change from baseline in the official diastolic blood pressure
Time frame: 1 year
Change from baseline in the official pulse pressure
Time frame: 1 year
Change from baseline in the official blood pressure compliance rate
Time frame: 1 year
New vascular events include ischemic stroke, TIA, cerebral hemorrhage, MI, pulmonary embolism, thrombosis, peripheral arterial occlusion
Time frame: 1 year
Numbers in all-cause hospitalization
Contact information is provided by the study sponsor or research team.
Dongzhimen Hospital, Beijing
Other
Songling Xuemaikang Capsules for Cerebral Small Vessel Disease: A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Study
Acronym: SXC-CSVD
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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