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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.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

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);
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  • 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.

Mei Cui, Doctor contact

+86-21-52888160

cuimei@fudan.edu.cn

Limin Yang, Doctor contact

+86-311-85901748

383505858@qq.com

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.

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 groups in NCT06061692
Study groupRoleWhat they receive
Test groupExperimentalTongxinluo Capsule, 4 capsules/time, tid, p.o
Receives: Drug: Tongxinluo Capsule
Control groupPlacebo comparatorTongxinluo 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.

  1. 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)
  1. 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

  2. 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

  3. 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

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

    Change from baseline in Mini-Mental State Examination (MMSE)

    Measured: 1 year

  5. Change from baseline in Symbol Digit Modalities Test (SDMT) at 1 year;

    Change from baseline in Symbol Digit Modalities Test (SDMT)

    Measured: 1 year

  6. Change from baseline in Clinical Dementia Rating Scale (CDR) at 1 year;

    Change from baseline in Clinical Dementia Rating Scale (CDR)

    Measured: 1 year

  7. Change from baseline in Neuropsychiatric Inventory Questionnaire (NPI-Q) at 1 year;

    Change from baseline in Neuropsychiatric Inventory Questionnaire (NPI-Q)

    Measured: 1 year

  8. 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

  9. 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.

  1. First posted29 Sep 2023
  2. Study startOct 2023 (estimated)
  3. Primary completionJun 2026 (estimated)
  4. Study completionDec 2026 (estimated)

Resources

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)
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

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.

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