Cerebral Small Vessel DiseasesPhase 4NCT06061692
Tongxinluo Capsule in the Treatment of Cerebral Small Vessel Disease-A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Study(TOPS-CSVD)
A Phase 4 study testing Tongxinluo Capsule in people with Cerebral Small Vessel Diseases, run by Fudan University.
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… Read more about this study
- Who is it for?
- Ages 50 to 80 years
- Conditions the study is for
- Cerebral Small Vessel Diseases
- What is being tested?
- Tongxinluo Capsule
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 1,052 participants
- Where
- No sites listed yet
- Study dates
- Oct 2023to Dec 2026
- Phase
- Phase 4
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 50 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age 50-80 years (both inclusive);
- Complaints of cognitive impairment involving memory and/or other cognitive domains for at least 3 months;
- 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;
- MRI has: ① 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. ② 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.);
- Voluntary participation in the study and willing to sign the Informed Consent Form.
Who cannot join
- Previously diagnosed with dementia;
- Acute stroke event within 6 months;
- Previously diagnosed hereditary or inflammatory small vessel disease;
- Presence of congenital mental retardation and severe neurological and psychiatric diseases;
- Illiterate or severe visual or hearing impairment that may prevent patients from cooperating with neuropsychological assessment;
- Relevant depression (Hamilton Depression Scale score ≥ 17 points), or other unrelated serious mental illness (schizophrenia, bipolar disorder or delirium);
Show all 12Show fewer
- 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);
- Alcohol abuse, drug abuse or use of drugs affecting cognitive assessment, such as sedatives, hypnotics, nootropic drugs, cholinergic drugs;
- Definitely diagnosed malignant tumor, vital organ failure;
- Previous allergy or intolerance to Tongxinluo ingredients;
- 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;
- Patients who have participated in other interventional clinical studies within the last 3 months, or are participating in other interventional clinical studies.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Tongxinluo Capsule in the Treatment of Cerebral Small Vessel Disease-A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Study (TOPS-CSVD)
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.
Read more
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.
- Conditions
- Cerebral Small Vessel Diseases
- Being tested
- Tongxinluo Capsule
- Keywords
- Cerebral Small Vessel Diseases, cognitive impairment
- Medical subject headings
- Cerebral Small Vessel Diseases, Cognitive Dysfunction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Tongxinluo CapsuleDrug
4 capsules/time, tid, p.o Duration of Treatment: 1 year (12 months)
| Study group | Role | What they receive |
|---|---|---|
| Test group | Experimental | Tongxinluo Capsule, 4 capsules/time, tid, p.o Receives: Drug: Tongxinluo Capsule |
| Control group | Placebo comparator | Tongxinluo Capsule placebo, 4 capsules/time, tid, p.o Receives: Drug: Tongxinluo Capsule |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in Vascular Dementia Cognitive Assessment Scale (VADAS-cog) at 1 year.
Changes in Vascular Dementia Cognitive Assessment Scale (VADAS-cog)
Measured: 1 year
Secondary outcomes (9)
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;
Measured: 1 year
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
Measured: 1 year
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)
Measured: 1 year
Change from baseline in Mini-Mental State Examination (MMSE) at 1 year;
Change from baseline in Mini-Mental State Examination (MMSE)
Measured: 1 year
Change from baseline in Symbol Digit Modalities Test (SDMT) at 1 year;
Change from baseline in Symbol Digit Modalities Test (SDMT)
Measured: 1 year
Change from baseline in Clinical Dementia Rating Scale (CDR) at 1 year;
Change from baseline in Clinical Dementia Rating Scale (CDR)
Measured: 1 year
Change from baseline in Neuropsychiatric Inventory Questionnaire (NPI-Q) at 1 year;
Change from baseline in Neuropsychiatric Inventory Questionnaire (NPI-Q)
Measured: 1 year
Change from baseline in Activity of Daily Living Scale (ADL) at 1 year;
Change from baseline in Activity of Daily Living Scale (ADL)
Measured: 1 year
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)
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Sep 2023
- Study startOct 2023 (estimated)
- Primary completionJun 2026 (estimated)
- Study completionDec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Cerebral Small Vessel DiseasesStudies of the same condition, open and under way.
- More trials run by Fudan UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 1,052 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Fudan University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Qiang Dong, Huashan Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06061692
- Sponsor's protocol ID
- TOPS-CSVD
- Status last verified
- Sep 2023
- First submitted
- 25 Sep 2023
- Last updated
- 29 Sep 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: The IPD will not share for confidentiality reasons
Publications
Wang Y, Xie X, Xu J, Lei P, Wang K, Zhang J, Yu J, Cui M, Dong Q. Tongxinluo capsule in the treatment of cerebral small vessel disease: protocol of a randomised, double-blind, placebo-controlled, multicentre clinical study (TOPS-CSVD). Stroke Vasc Neurol. 2026 Apr 27;11(2):253-260. doi: 10.1136/svn-2024-003929.
PubMed 40935402
Study at a glance
From the registry record, last updated by the sponsor on 29 Sep 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Tongxinluo Capsule in the Treatment of Cerebral Small Vessel Disease-A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Study (TOPS-CSVD)
- ClinicalTrials.gov ID
- NCT06061692
- Acronym / sponsor ID
- TOPS-CSVD
- Conditions
- Cerebral Small Vessel Diseases
- Keywords
- Cerebral Small Vessel Diseases, cognitive impairment
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 1,052 participants (estimated)
- Lead sponsor
- Fudan UniversityUniversity, hospital or other
- Study start
- Oct 2023 (estimated)
- Primary completion
- Jun 2026 (estimated)
- Study completion
- Dec 2026 (estimated)
- First posted
- 29 Sep 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Test group | Experimental | Drug: Tongxinluo CapsuleTongxinluo Capsule, 4 capsules/time, tid, p.o |
| Control group | Placebo comparator | Drug: Tongxinluo CapsuleTongxinluo Capsule placebo, 4 capsules/time, tid, p.o |
Who may qualify
- Ages
- 50 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Age 50-80 years (both inclusive);
- Complaints of cognitive impairment involving memory and/or other cognitive domains for at least 3 months;
- 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;
- MRI has: ① 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. ② 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.);
- Voluntary participation in the study and willing to sign the Informed Consent Form.
Key exclusion criteria (12 listed)
- Previously diagnosed with dementia;
- Acute stroke event within 6 months;
- Previously diagnosed hereditary or inflammatory small vessel disease;
- Presence of congenital mental retardation and severe neurological and psychiatric diseases;
- Illiterate or severe visual or hearing impairment that may prevent patients from cooperating with neuropsychological assessment;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Tongxinluo Capsule4 capsules/time, tid, p.o Duration of Treatment: 1 year (12 months) | Drug | Control group, Test group |
Primary outcome
Changes in Vascular Dementia Cognitive Assessment Scale (VADAS-cog) at 1 year.
Time frame: 1 year
Changes in Vascular Dementia Cognitive Assessment Scale (VADAS-cog)
9 secondary outcomes
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;
Time frame: 1 year
The incidence rate of each individual event of the combined endpoint at 1 year;
Time frame: 1 year
Changes in Clinician Interview-Based Impression of Change Scale (CIBIC-Plus) at 1 year;
Time frame: 1 year
Change from baseline in Mini-Mental State Examination (MMSE) at 1 year;
Time frame: 1 year
Change from baseline in Symbol Digit Modalities Test (SDMT) at 1 year;
Time frame: 1 year
Change from baseline in Clinical Dementia Rating Scale (CDR) at 1 year;
Time frame: 1 year
Change from baseline in Neuropsychiatric Inventory Questionnaire (NPI-Q) at 1 year;
Time frame: 1 year
Change from baseline in Activity of Daily Living Scale (ADL) at 1 year;
Time frame: 1 year
Change from baseline in motor score (TUG, 3-meter walking time) at 1 year;
Time frame: 1 year
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Sep 2023.
- Derived from this study: PubMed 40935402Wang Y, Xie X, Xu J, Lei P, Wang K, Zhang J, Yu J, Cui M, Dong Q. Tongxinluo capsule in the treatment of cerebral small vessel disease: protocol of a randomised, double-blind, placebo-controlled, multicentre clinical study (TOPS-CSVD). Stroke Vasc Neurol. 2026 Apr 27;11(2):253-260. doi: 10.1136/svn-2024-003929.
- Individual participant dataSharing planned: No. The IPD will not share for confidentiality reasons
Related trials for Cerebral Small Vessel Diseases
RecruitingPhase 3
Treatment of Acute Ischemic Stroke With Edaravone Dexborneol Sublingual Tablets in Small Vessel Disease
Cerebral Small Vessel Disease, Ischemic Stroke
Not yet recruitingObservational study
Continuous Blood Pressure Variability and Small Vessel Disease in Acute Ischemic Stroke
Ischemic Stroke, Acute, Blood Pressure Variability
Not yet recruiting
Personalized Intermittent Theta Burst Stimulation for Cognitive Impairment Related to Cerebral Small Vessel Disease
Cerebral Small Vessel Disease, Vascular Cognitive Impairment
Not yet recruitingObservational study
Outcome Prediction and Recovery After Spontaneous Intracerebral Haemorrhage
Intracerebral Hemorrhage, Hemorrhagic Stroke
Not yet recruitingObservational study
Study on Eye-Brain Cross-Organ Mapping and Systemic Disease Association Based on Multimodal Big Data
Cataract, Vitreous Hemorrhage
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Tongxinluo Capsule in people with Cerebral Small Vessel Diseases, run by Fudan University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 29 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mei Cui, Doctor (+86-21-52888160, cuimei@fudan.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in Vascular Dementia Cognitive Assessment Scale (VADAS-cog) at 1 year. (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06061692, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Sep 2023; AzTrials last refreshed its copy on 8 Nov 2026.