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NCT Number: NCT07121088

Traditional Chinese Medicine Intervention for Ischemic Cerebrovascular Disease and Diabetes Mellitus: An Efficacy Comparative Study

The objective of this observational study is to understand the long-term effects of traditional Chinese medicine (TCM) intervention on patients with cerebral infarction onset within <48 hours and comorbid diabetes. The primary question it aims to address is:

Can long-term TCM intervention for the treatment of ischemic cerebrovascular disease comorbid with diabetes improve patients' neurological deficits and self-care ability? Participants receiving TCM intervention (universal treatment combined with syndrome-specific treatment) as part of routine cerebrovascular disease management will undergo follow-up assessments at 30 days, 90 days, 6 months, and 12 months within 1 year to evaluate neurological status (e.g., mRS score, NIHSS score) and quality of life indicators.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

About this study

The population with ischemic cerebrovascular disease (ICVD) comorbid with diabetes is growing, characterized by high mortality, disability, and recurrence rates of vascular events, with a lack of effective treatments. There are 529 million diabetic patients worldwide and 129 million in China, among which 43 million have comorbid vascular diseases; China has approximately 10 million ischemic stroke patients, with 4.5 million comorbid diabetes. Diabetes increases the risk of ischemic stroke, and the proportion of deaths related to diabetic cerebrovascular diseases has risen significantly. Polypharmacy also raises the risk of adverse drug interactions, imposing a heavy medical burden.

The pathological mechanism aligns with the TCM theory of "toxin damaging collaterals": Diabetes-induced glucose/lipid metabolism disorders and activation of the renin-angiotensin-aldosterone system cause systemic vascular endothelial dysfunction and atherosclerosis. Macrovascular lesions mainly involve atherosclerosis, while microvascular lesions include endothelial damage and microcirculatory disorders, with core mechanisms involving energy metabolism abnormalities and mitochondrial dysfunction. TCM holds that "excessive pathogens transform into toxins," and toxin-induced collateral damage disrupts structure and function, consistent with the above pathology. Thus, "detoxification and collaterals dredging" (combining qi-nourishing, blood-activating, and stasis-removing) is the core therapeutic principle.

Chuanzhi Tongluo Capsules (Lunan Pharmaceutical), a Shandong famous brand with annual sales over 100 million yuan, exert effects of promoting blood circulation and dredging collaterals, reducing inflammation and improving microcirculation. This project explores a TCM program combining "acute-phase intensive treatment + recovery-phase sequential treatment" and "universal + syndrome-specific treatment." Entitled Comparative Efficacy Study of TCM Intervention in ICVD Comorbid with Diabetes, this Phase IV trial spans 4 years, adopting a multi-center real-world non-randomized controlled design. It will enroll 3,666 patients with acute cerebral infarction (onset <48h) comorbid diabetes across 50 centers. The control group receives standard secondary prevention of cerebrovascular disease and hypoglycemic treatment; the trial group adds Chuanzhi Tongluo Capsules (4 capsules thrice daily for 14 days, then 2 capsules thrice daily for 1 year) plus syndrome-specific treatment (5 TCM syndromes with corresponding herbs for 14 days).

Inclusion criteria

≥18 years old, meeting diabetes/acute ischemic stroke criteria, and TCM "toxin damaging brain collaterals" syndrome. Exclusions: hemorrhagic transformation, large infarction, type 1 diabetes, etc. The primary endpoint is the proportion of patients with mRS 0-2 at 90 days. Secondary endpoints include 1-year BARC type III/V major bleeding, MACCE, all-cause mortality, diabetic microvascular lesions (renal indices), mRS, MMSE, and EQ-5D-5L at 6/12 months. Data are managed via EpiData and analyzed with SAS, using chi-square test, t-test, and rank sum test, with 90% statistical power (α=0.05, β=0.10). The trial aims to establish a "disease-syndrome combined" long-term intervention model, expanding TCM applicability and evidence generalization.

English Abbreviation The population with ischemic cerebrovascular disease (ICVD) comorbid with diabetes is growing, with high mortality, disability, and recurrence rates of vascular events, and a lack of effective treatments. Globally, there are 529 million diabetic patients, including 129 million in China, among whom 43 million have comorbid vascular diseases; China has ~10 million ischemic stroke patients, with ~4.5 million comorbid diabetes. Diabetes elevates ischemic stroke risk, and related deaths are increasing, while polypharmacy raises adverse interactions and medical burdens.

Pathologically, it aligns with TCM's "toxin damaging collaterals" theory: Diabetes-induced metabolic disorders and systemic vascular activation cause endothelial dysfunction and atherosclerosis (macrovascular lesions) and microcirculatory disorders (microvascular lesions), involving energy metabolism and mitochondrial dysfunction. TCM holds toxins damage collaterals, disrupting structure/function, consistent with the pathology, so "detoxification and collaterals dredging" (combining qi-nourishing, blood-activating) is key.

Chuanzhi Tongluo Capsules (Lunan Pharmaceutical), a Shandong famous brand with annual sales over ¥100 million, improve circulation and reduce inflammation. This Phase IV trial (4 years) uses a multi-center real-world non-randomized design, enrolling 3,666 patients (onset <48h) across 50 centers. The control group receives standard care; the trial group adds Chuanzhi Tongluo Capsules (intensive: 4 caps thrice daily for 14 days; sequential: 2 caps thrice daily for 1 year) plus syndrome-specific herbs for 5 TCM syndromes.

Inclusion: ≥18 years, meeting diabetes/ischemic stroke criteria, and "toxin damaging brain collaterals" syndrome. Exclusions: hemorrhagic transformation, large infarction, type 1 diabetes, etc. Primary endpoint: 90-day mRS 0-2 proportion. Secondary endpoints: 1-year BARC III/V bleeding, MACCE, mortality, diabetic microvascular lesions, mRS, MMSE, EQ-5D-5L at 6/12 months. Analyzed via EpiData and SAS (chi-square, t-test, rank sum test) with 90% power (α=0.05, β=0.10). It aims to establish a "disease-syndrome combined" model, expanding TCM applicability and evidence generalization.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years old, regardless of gender.
  • Previously diagnosed with diabetes, or with an unknown medical history, meeting the WHO 2023 diagnostic criteria for type 2 diabetes, including any of the following:
  • Fasting blood glucose ≥ 7.0 mmol/L.
  • 2-hour postprandial blood glucose ≥ 11.1 mmol/L.
  • Glycated hemoglobin ≥ 6.5%.
  • Acute cerebral infarction meets the diagnostic criteria of *Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2023*:
  • Acute onset.
  • Focal neurological deficits, with a few cases showing global neurological deficits.
  • The presence of a responsible lesion on imaging or symptoms/signs persisting for more than 24 hours.
  • Exclusion of non-vascular etiologies.
  • Exclusion of intracerebral hemorrhage by brain CT/MRI.
  • Onset of cerebral infarction < 48 hours.
  • TCM syndrome conforms to the "toxin damaging brain collaterals" syndrome (referring to the diagnostic criteria (draft) of *Research on the Diagnostic Criteria for the Syndrome of Mutual Binding of Stasis and Toxin in Ischemic Cardiovascular and Cerebrovascular Diseases* (Ju Jianqing et al., 2023)).
  • Modified Rankin Scale (mRS) before onset: 0 - 1 point.
  • National Institutes of Health Stroke Scale (NIHSS) at admission: 4 - 24 points.
  • Signed informed consent form.

Treatment and study plan

(Intensive treatment) Chuanzhi Tongluo Capsules

Drug

4 capsules each time, orally, 3 times a day; administration from day 1 to day 14 of the disease.

Standard Treatment (Guideline-Based)

Other

Combination therapy including: 1. Antiplatelet: aspirin 100 mg/day + clopidogrel 75 mg/day. 2. Lipid-lowering: atorvastatin 20 mg/day. 3. Antidiabetic: metformin 500 mg bid (max 2000 mg/day). *Doses may be adjusted per local guidelines or patient tolerance.

(Sequential treatment) Chuanzhi Tongluo Capsules

Drug

2 capsules each time, orally, 3 times a day; administration from day 15 to day 365.

TCM Syndrome Differentiation Decoction

Drug

Individualized herbal decoction based on TCM diagnosis (four diagnostic methods), administered for 14 days during intensive phase.

Primary outcomes

  1. Primary outcome indicator

    Time frame: 90days

    The proportion of patients with mRS score 0-2 at 90 days

Secondary outcomes

  1. BARC Type III and V Major Bleeding (Incidence %)

    Time frame: 1year

    The percentage of patients meeting the following criteria: Type IIIa is overt bleeding with a hemoglobin drop of 3-<5 g/dL or requiring transfusion; Type IIIb is a hemoglobin drop of >5 g/dL, cardiac tamponade, bleeding requiring surgical intervention (excluding dental/nasal/skin/hemorrhoidal bleeding), or requiring intravenous vasoactive drugs; Type IIIc is intracranial/spinal hemorrhage (excluding microhemorrhage/hemorrhagic transformation); Type V is fatal bleeding.

  2. 1-Year Major Adverse Cardiovascular and Cerebrovascular Events (MACCEs) (Cumulative Incidence %)

    Time frame: 1year

    The percentage of patients who experience major adverse cardiovascular and cerebrovascular events (in accordance with international criteria: including myocardial infarction, recurrent stroke, cardiovascular death, etc.) within 1 year.

  3. 1-Year All-Cause Mortality (Mortality Rate %)

    Time frame: 1year

    The percentage of patients who die from any cause within 1 year after treatment.

Other outcomes

  1. Rate of Change in eGFR (mL/min/1.73 m²/year)

    Time frame: Baseline, 6 months, 12 months

    Estimated glomerular filtration rate (eGFR) calculated using CKD-EPI formula. Annualized rate of change derived from serial measurements at baseline, 6, and 12 months.

  2. 12-month Renal Composite Endpoint

    Time frame: 12 months

    Composite of: 1) Sustained ≥50% decline in eGFR from baseline; 2) Sustained eGFR <15 mL/min/1.73 m²; 3) Initiation of long-term dialysis or renal transplantation.

  3. Rate of Change in UACR (mg/g/year)

    Time frame: Baseline, 6 months, 12 months

    Urine albumin-to-creatinine ratio (UACR) measured from first-morning void samples. Annualized rate of change calculated from baseline, 6, and 12-month data.

  4. Change in Tubular Markers (α1-MG, β2-MG, NAG) at 12 Months

    Time frame: Baseline, 12 months

    Urinary biomarkers of tubular injury: α1-microglobulin (α1-MG), β2-microglobulin (β2-MG), and N-acetyl-β-D-glucosaminidase (NAG). Concentrations measured by immunoturbidimetry (α1-MG, β2-MG) and enzymatic assay (NAG).

Study contacts

Contact information is provided by the study sponsor or research team.

Tao Huang, doctor

CONTACT

[email protected]

18688898958

zheng zhen, master

CONTACT

[email protected]

19120517600

Sponsors and collaborators

Lead sponsor

Guangzhou University of Traditional Chinese Medicine

Other

Registry information

Official study title

Comparative Effectiveness Study of Traditional Chinese Medicine Intervention in Ischemic Cerebrovascular Disease Comorbid With Diabetes Mellitus

Acronym: TIDES

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Aug 13, 2025
Registry last updated
Aug 13, 2025

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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