Tongxinluo Capsule in the Treatment of Cerebral Small Vessel Disease-A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Study（TOPS-CSVD）

Cerebral Small Vessel Diseases Clinical Trial

Official title:

Tongxinluo Capsule in the Treatment of Cerebral Small Vessel Disease-A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Study (TOPS-CSVD)

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06061692
• Other study ID #: TOPS-CSVD
• Status: Not yet recruiting
• Phase: Phase 4
• Start date: October 2023
• Est. completion date: December 2026

Study information

• Verified date: September 2023
• Source: Fudan University
• Contact: Mei Cui, Doctor
• Phone: +86-21-52888160
• Email: cuimei[@]fudan.edu.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Cerebral small vessel disease is a series of clinical, imaging and pathological syndromes caused by various etiologies affecting the arteries, capillaries, venules in the brain. The common causes of cerebral small vessel disease include arteriolosclerosis, cerebral amyloid angiopathy, hereditary cerebral small vessel disease, inflammation-and immune-mediated small vessel disease, venous collagen disease and other small vessel diseases. Of these, age-and hypertension-related cerebral small vessel disease and amyloidosis cerebral small vessel disease are the most common types. The pathophysiological mechanism and clinical manifestations of cerebral small vessel disease are complex. One-fifth of ischemic strokes and the vast majority of nontraumatic parenchymal hemorrhages are due to cerebral small vessel disease. In addition to stroke, patients with cerebral small vessel disease are more often characterized by chronic progressive neurological impairment, which is an important cause of cognitive decline and functional disability in the elderly, and has become one of the important public health problems affecting the quality of life of the elderly. Focusing on cognitive impairment-related diseases, a large number of clinical studies have shown that Tongxinluo capsule has a dual neurovascular protective effect, which can increase the Mini-Mental State Examination (MMSE) score and activities of daily living (ADL) score of patients with lacunar cerebral infarction combined with vascular cognitive impairment, reduce fibrinogen (FIB) concentration, improve whole blood viscosity, improve blood viscosity and FIB level, improve activities of daily living and accelerate intellectual recovery in patients with VD; It can also reduce the levels of ET-1 and homocysteine in AD patients, reduce the whole blood viscosity and thus improve the microcirculation in the elderly, increase cerebral blood flow, increase the scores of MMSE and ADL, improve the intelligence of patients, improve memory disorders and language disorders. Meta-analysis of 3458 patients in 40 published clinical literatures of Tongxinluo capsule both domestically and internationally confirmed that Tongxinluo capsule had the effect of promoting the recovery of neurological function, and was safe without adverse reactions. This project is a randomized, double-blind, placebo-controlled multicenter clinical study to investigate the clinical efficacy and safety of Tongxinluo capsule in the treatment of cerebral small vessel disease. A total of 1052 subjects who met the subject screening criteria are planned to be enrolled, with 526 patients in the test group and 526 patients in the placebo group. The study is conducted using a central randomization method. For the patients who met the inclusion criteria after examination, they are logged into the Interactive Web Response System by their site, entered the relevant information, and randomized and assigned drugs automatically by the central server according to the ratio of 1:1. Once enrolled, all patients receive the study drug (Tongxinluo or placebo) at 4 capsules/tid for up to 12 months. The study is planned to be conducted at approximately 50 centers across the country using central randomized competing enrollment.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 1052
• Est. completion date: December 2026
• Est. primary completion date: June 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 50 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Age 50-80 years (both inclusive);

2. Complaints of cognitive impairment involving memory and/or other cognitive domains for at least 3 months;

3. Neither normal nor demented cognitive level according to DSM-V criteria, MMSE scale score =20 (elementary school) or =24 (junior high school and above); CDR scale score =0.5 in at least one domain and overall CDR score =1;

4. MRI has: ? moderate to severe white matter lesions (deep Fazekas score > 1 or paraventricular Fazekas score > 2); Mild white matter hyperintensity (deep Fazekas score = 1 or paraventricular Fazekas score = 2) combined with more than 1 lacunar infarction or more than 3 microbleeds foci. ? Absence of old cortical or watershed infarction, cerebral hemorrhage, hydrocephalus, and other cerebral white matter lesions of definite etiology (e.g., multiple sclerosis, metabolic, toxic, etc.);

5. Voluntary participation in the study and willing to sign the Informed Consent Form.

Exclusion Criteria:

1. Previously diagnosed with dementia;

2. Acute stroke event within 6 months;

3. Previously diagnosed hereditary or inflammatory small vessel disease;

4. Presence of congenital mental retardation and severe neurological and psychiatric diseases;

5. Illiterate or severe visual or hearing impairment that may prevent patients from cooperating with neuropsychological assessment;

6. Relevant depression (Hamilton Depression Scale score = 17 points), or other unrelated serious mental illness (schizophrenia, bipolar disorder or delirium);

7. Combined with severe cardiac, pulmonary and renal insufficiency (creatinine > 2.0 mg/dL or 177 µmol/L), severe hepatic impairment (transaminase more than 3 times of normal value);

8. Alcohol abuse, drug abuse or use of drugs affecting cognitive assessment, such as sedatives, hypnotics, nootropic drugs, cholinergic drugs;

9. Definitely diagnosed malignant tumor, vital organ failure;

10. Previous allergy or intolerance to Tongxinluo ingredients;

11. The subject has no stable and reliable caregiver, or the caregiver is unable to help the subject participate in the whole process of the study;

12. Patients who have participated in other interventional clinical studies within the last 3 months, or are participating in other interventional clinical studies.

Related Conditions & MeSH terms

• Cerebral Small Vessel Diseases

Intervention

Drug:
• Tongxinluo Capsule
4 capsules/time, tid, p.o Duration of Treatment: 1 year (12 months)

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Fudan University

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Volume changes in brain regions at 1 year;	Volume changes in brain regions	1 year
Other	Volume changes in cerebral white matter at 1 year;	Volume changes in cerebral white matter	1 year
Other	Changes in number of cerebral microbleeds at 1 year;	Changes in number of cerebral microbleeds	1 year
Other	Changes of cerebral blood flow at 1 year.	Changes of cerebral blood flow.	1 year
Primary	Changes in Vascular Dementia Cognitive Assessment Scale (VADAS-cog) at 1 year.	Changes in Vascular Dementia Cognitive Assessment Scale (VADAS-cog)	1 year
Secondary	Incidence rate of combined endpoint at 1 year: including new stroke (ischemic [TOAST classification] or hemorrhagic)/transient ischemic attack, myocardial infarction, new dementia and death;	Incidence rate of combined endpoint at 1 year: including new stroke (ischemic [TOAST classification] or hemorrhagic)/transient ischemic attack, myocardial infarction, new dementia and death;	1 year
Secondary	The incidence rate of each individual event of the combined endpoint at 1 year;	The incidence rate of each individual event of the combined endpoint	1 year
Secondary	Changes in Clinician Interview-Based Impression of Change Scale (CIBIC-Plus) at 1 year;	Changes in Clinician Interview-Based Impression of Change Scale (CIBIC-Plus)	1 year
Secondary	Change from baseline in Mini-Mental State Examination (MMSE) at 1 year;	Change from baseline in Mini-Mental State Examination (MMSE)	1 year
Secondary	Change from baseline in Symbol Digit Modalities Test (SDMT) at 1 year;	Change from baseline in Symbol Digit Modalities Test (SDMT)	1 year
Secondary	Change from baseline in Clinical Dementia Rating Scale (CDR) at 1 year;	Change from baseline in Clinical Dementia Rating Scale (CDR)	1 year
Secondary	Change from baseline in Neuropsychiatric Inventory Questionnaire (NPI-Q) at 1 year;	Change from baseline in Neuropsychiatric Inventory Questionnaire (NPI-Q)	1 year
Secondary	Change from baseline in Activity of Daily Living Scale (ADL) at 1 year;	Change from baseline in Activity of Daily Living Scale (ADL)	1 year
Secondary	Change from baseline in motor score (TUG, 3-meter walking time) at 1 year;	Change from baseline in motor score (TUG, 3-meter walking time)	1 year