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- Ensayo clínico NCT07613060
Establishment of Disease Characteristics and a Chinese Medicine Prognosis Risk Model Based on a Large-Scale Database After Coronary Revascularization
Descripción general del estudio
Estado
Descripción detallada
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.
Tipo de estudio
Inscripción (Estimado)
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Liu Qiang
- Número de teléfono: 13588121905
- Correo electrónico: 19981011@zcmu.com
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Método de muestreo
Población de estudio
Descripción
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
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
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Adults post-coronary revascularization.
Patients aged ≥18 years who underwent coronary revascularization (PCI or CABG).
Consecutive enrollment from 5 Chinese hospitals.
Prospective follow-up at 12, 24, 36, and 48 weeks post-enrollment.
Assessments include MACE (all-cause death, stent thrombosis, myocardial infarction, unstable angina, repeat revascularization, rehospitalization), TCM syndrome score, NYHA class, echocardiography, ambulatory ECG, and biospecimens (blood and tongue coating for proteomics, metabolomics, microbiomics).
No intervention is assigned.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Major Adverse Cardiovascular Events (MACE)
Periodo de tiempo: 12, 24, 36, and 48 weeks post-enrollment
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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.
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12, 24, 36, and 48 weeks post-enrollment
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Traditional Chinese Medicine (TCM) Syndrome Score
Periodo de tiempo: Baseline, 12, 24, 36, 48 weeks post-enrollment
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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
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Baseline, 12, 24, 36, 48 weeks post-enrollment
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NYHA Functional Class
Periodo de tiempo: 12, 24, 36, 48 weeks post-enrollment
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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
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12, 24, 36, 48 weeks post-enrollment
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Multi-omics Biomarkers (exploratory)
Periodo de tiempo: Baseline
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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
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Baseline
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Left Ventricular End-Diastolic Diameter (LVEDD)
Periodo de tiempo: Baseline
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Diameter of the left ventricle at end-diastole, measured by echocardiography.
Unit of Measure: mm.
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Baseline
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Left Ventricular End-Systolic Diameter (LVESD)
Periodo de tiempo: Baseline
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Diameter of the left ventricle at end-systole, measured by echocardiography.
Unit of Measure: mm
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Baseline
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Left Ventricular Posterior Wall Thickness (LVPW)
Periodo de tiempo: Baseline
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Thickness of the left ventricular posterior wall in diastole, measured by echocardiography.
Unit of Measure: mm.
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Baseline
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Interventricular Septal Thickness (IVS)
Periodo de tiempo: Baseline
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Thickness of the interventricular septum in diastole, measured by echocardiography.
Unit of Measure: mm
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Baseline
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Left Ventricular Ejection Fraction (LVEF)
Periodo de tiempo: Baseline
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Percentage of blood ejected from the left ventricle per contraction, measured by echocardiography.
Unit of Measure: %.
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Baseline
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Left Ventricular Fractional Shortening (FS)
Periodo de tiempo: Baseline
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Percentage change in left ventricular diameter between diastole and systole, measured by echocardiography.
Unit of Measure: %
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Baseline
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E/A Ratio
Periodo de tiempo: Baseline
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Ratio of early (E) to late (A) ventricular filling velocities, measured by pulsed-wave Doppler echocardiography.
Unit of Measure: ratio
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Baseline
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Mean Heart Rate (24-hour)
Periodo de tiempo: Baseline
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Average heart rate over 24 hours derived from ambulatory electrocardiography (Holter).
Unit of Measure: beats per minute (bpm)
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Baseline
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Minimum Heart Rate (24-hour)
Periodo de tiempo: Baseline
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Lowest heart rate recorded during 24-hour ambulatory ECG, with timestamp.
Unit of Measure: bpm.
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Baseline
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Maximum Heart Rate (24-hour)
Periodo de tiempo: Baseline
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Highest heart rate recorded during 24-hour ambulatory ECG, with timestamp.
Unit of Measure: bpm.
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Baseline
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Total Premature Ventricular Contractions (PVCs)
Periodo de tiempo: Baseline
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Number of premature ventricular contractions recorded over 24 hours by ambulatory ECG.
Unit of Measure: count per 24h
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Baseline
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Total Premature Atrial Contractions (PACs)
Periodo de tiempo: Baseline
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Number of premature atrial contractions recorded over 24 hours by ambulatory ECG.
Unit of Measure: count per 24h
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Baseline
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Maximum RR Interval
Periodo de tiempo: Baseline
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Longest interval between two consecutive R waves on 24-hour ambulatory ECG, indicating cardiac pause.
Unit of Measure: seconds (s)
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Baseline
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ST Segment Depression Maximum Amplitude
Periodo de tiempo: Baseline
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Greatest magnitude of ST segment depression during any ischemic event on 24-hour ambulatory ECG.
Unit of Measure: mm (or mV)
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Baseline
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ST Segment Depression Longest Duration
Periodo de tiempo: Baseline
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Longest duration of a single ST segment depression event on 24-hour ambulatory ECG.
Unit of Measure: minutes (min)
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Baseline
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SDNN (Heart Rate Variability)
Periodo de tiempo: Baseline
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Standard deviation of all normal-to-normal R-R intervals over 24 hours, a measure of heart rate variability.
Unit of Measure: milliseconds (ms)
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Baseline
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
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Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- ZSLL-KY-2026-027-01
Plan de datos de participantes individuales (IPD)
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Descripción del plan IPD
Información sobre medicamentos y dispositivos, documentos del estudio
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