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NCT Number: NCT07613060

Establishment of Disease Characteristics and a Chinese Medicine Prognosis Risk Model Based on a Large-Scale Database After Coronary Revascularization

This study aims to develop a risk prediction model for patients who have undergone coronary revascularization (such as stent placement or bypass surgery). After these procedures, some patients still experience heart-related problems like chest pain, heart attack, or rehospitalization. This study will enroll 600 patients from multiple hospitals in China and follow them for 12 months. At enrollment and at 12, 24, 36, and 48 weeks after surgery, researchers will collect clinical information (including traditional Chinese medicine symptoms, blood tests, heart imaging) and biological samples (blood and tongue coating). Using artificial intelligence, the study will build a predictive model that combines Western medical data with traditional Chinese medicine characteristics. The goal is to better identify patients at higher risk of future heart events, so that personalized prevention and management can be provided. The study does not involve any experimental treatment or intervention - it is purely observational.

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Key information

About this study

This is a multicenter, prospective cohort study conducted at five sites in China. The study aims to develop and validate a prognostic risk model for major adverse cardiovascular events (MACE) in patients after coronary revascularization (percutaneous coronary intervention or coronary artery bypass grafting).

Study population: A total of 600 eligible patients aged ≥18 years who have undergone coronary revascularization will be enrolled consecutively. Key exclusion criteria include severe heart failure, malignant arrhythmias, severe pulmonary or liver/kidney dysfunction, pregnancy, psychiatric disorders, and poor compliance.

Data collection: At baseline (enrollment), the following data are collected: demographics, medical history, surgical characteristics (e.g., access route, number of stents, target vessels), vital signs, laboratory tests (complete blood count, cardiac enzymes, liver/kidney function, lipids, glucose), echocardiography, 24-hour ambulatory electrocardiography, and a standardized Traditional Chinese Medicine (TCM) case report form covering symptom scores, tongue/pulse findings, and pattern elements. In addition, biological samples (blood and tongue coating) are obtained for proteomics, metabolomics, and tongue-coating microbiomics.

Follow-up: Participants are followed at 12, 24, 36, and 48 weeks post-enrollment. At each follow-up, the TCM case report form is reassessed, MACE (including all-cause death, subacute stent thrombosis, perioperative myocardial infarction, recurrent myocardial infarction, recurrent unstable angina, repeat revascularization, and rehospitalization for angina or heart failure) are recorded, and NYHA functional class and current medications are updated.

Statistical analysis: Missing data will be handled by mean imputation or K-nearest neighbors imputation. Continuous variables will be standardized using Z-scores, and categorical variables will be one-hot encoded. Feature selection will be performed using LASSO regression. Three nested prediction models will be built:

  • Model_Base: Cox proportional hazards model based on routine clinical and imaging variables.
  • Model_TCM: adding TCM syndrome features using machine learning algorithms (random forest, support vector machine).
  • Model_Full: further integrating multi-omics biomarkers using deep learning methods (convolutional neural network, transformer).

Model performance will be assessed by discrimination (area under the ROC curve), calibration, and decision curve analysis. Internal validation will use k-fold cross-validation, and external validation will be conducted in at least three independent hospitals. The targeted predictive accuracy (area under the curve) is above 85%. All analyses will be performed using SPSS 26.0, Python, and R.

Ethics: The study protocol has been approved by the ethics committee of the lead site (The Third Affiliated Hospital of Zhejiang Chinese Medical University) and will be approved by participating centers. Written informed consent will be obtained from all participants.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis of coronary artery disease with prior coronary revascularization (PCI or CABG)
  • Age ≥ 18 years
  • Signed informed consent

Exclusion criteria

  • Malignant arrhythmias, severe heart failure, myocardial disease, or structural heart disease
  • Severe pulmonary insufficiency, severe liver or kidney dysfunction, severe electrolyte disturbances
  • Pregnancy or breastfeeding
  • Severe psychiatric disorders, malignant tumors, hematologic diseases, rheumatic immune diseases, or severe infection
  • Poor compliance or any other reason making the participant unsuitable for the study

Treatment and study plan

Primary outcomes

  1. Major Adverse Cardiovascular Events (MACE)

    Time frame: 12, 24, 36, and 48 weeks post-enrollment

    Composite of all-cause death, subacute stent thrombosis, perioperative myocardial infarction, recurrent myocardial infarction, recurrent unstable angina, repeat revascularization (PCI or CABG), and rehospitalization due to angina or heart failure. Events are ascertained by medical records, clinical diagnosis, coronary angiography, ECG, and cardiac enzyme/troponin measurements.

Secondary outcomes

  1. Traditional Chinese Medicine (TCM) Syndrome Score

    Time frame: Baseline, 12, 24, 36, 48 weeks post-enrollment

    Total score of TCM symptoms and signs (chest pain, palpitations, fatigue, tongue/pulse, etc.). Each item scored 0-3 (none to severe). Sum of all items. Higher score indicates more severe symptoms. Unit of Measure: points on a scale

  2. NYHA Functional Class

    Time frame: 12, 24, 36, 48 weeks post-enrollment

    Classification of heart failure symptoms based on physical activity limitation. Class I (no limitation) to IV (symptoms at rest). Unit of Measure: relative abundance / qualitative

  3. Multi-omics Biomarkers (exploratory)

    Time frame: Baseline

    Proteomics, metabolomics (LC-MS/MS, LC-MS/GC-MS) from blood, and 16S rRNA microbiome from tongue coating. Used to identify biomarkers associated with TCM patterns. Results reported as relative abundance or presence/absence. Unit of Measure: relative abundance / qualitative

  4. Left Ventricular End-Diastolic Diameter (LVEDD)

    Time frame: Baseline

    Diameter of the left ventricle at end-diastole, measured by echocardiography. Unit of Measure: mm.

  5. Left Ventricular End-Systolic Diameter (LVESD)

    Time frame: Baseline

    Diameter of the left ventricle at end-systole, measured by echocardiography. Unit of Measure: mm

  6. Left Ventricular Posterior Wall Thickness (LVPW)

    Time frame: Baseline

    Thickness of the left ventricular posterior wall in diastole, measured by echocardiography. Unit of Measure: mm.

  7. Interventricular Septal Thickness (IVS)

    Time frame: Baseline

    Thickness of the interventricular septum in diastole, measured by echocardiography. Unit of Measure: mm

  8. Left Ventricular Ejection Fraction (LVEF)

    Time frame: Baseline

    Percentage of blood ejected from the left ventricle per contraction, measured by echocardiography. Unit of Measure: %.

  9. Left Ventricular Fractional Shortening (FS)

    Time frame: Baseline

    Percentage change in left ventricular diameter between diastole and systole, measured by echocardiography. Unit of Measure: %

  10. E/A Ratio

    Time frame: Baseline

    Ratio of early (E) to late (A) ventricular filling velocities, measured by pulsed-wave Doppler echocardiography. Unit of Measure: ratio

  11. Mean Heart Rate (24-hour)

    Time frame: Baseline

    Average heart rate over 24 hours derived from ambulatory electrocardiography (Holter). Unit of Measure: beats per minute (bpm)

  12. Minimum Heart Rate (24-hour)

    Time frame: Baseline

    Lowest heart rate recorded during 24-hour ambulatory ECG, with timestamp. Unit of Measure: bpm.

  13. Maximum Heart Rate (24-hour)

    Time frame: Baseline

    Highest heart rate recorded during 24-hour ambulatory ECG, with timestamp. Unit of Measure: bpm.

  14. Total Premature Ventricular Contractions (PVCs)

    Time frame: Baseline

    Number of premature ventricular contractions recorded over 24 hours by ambulatory ECG. Unit of Measure: count per 24h

  15. Total Premature Atrial Contractions (PACs)

    Time frame: Baseline

    Number of premature atrial contractions recorded over 24 hours by ambulatory ECG. Unit of Measure: count per 24h

  16. Maximum RR Interval

    Time frame: Baseline

    Longest interval between two consecutive R waves on 24-hour ambulatory ECG, indicating cardiac pause. Unit of Measure: seconds (s)

  17. ST Segment Depression Maximum Amplitude

    Time frame: Baseline

    Greatest magnitude of ST segment depression during any ischemic event on 24-hour ambulatory ECG. Unit of Measure: mm (or mV)

  18. ST Segment Depression Longest Duration

    Time frame: Baseline

    Longest duration of a single ST segment depression event on 24-hour ambulatory ECG. Unit of Measure: minutes (min)

  19. SDNN (Heart Rate Variability)

    Time frame: Baseline

    Standard deviation of all normal-to-normal R-R intervals over 24 hours, a measure of heart rate variability. Unit of Measure: milliseconds (ms)

Study contacts

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

Liu Qiang

CONTACT

[email protected]

13588121905

Sponsors and collaborators

Lead sponsor

Liu Qiang

Other

Registry information

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
May 29, 2026
Registry last updated
May 29, 2026

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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