- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07613060
Establishment of Disease Characteristics and a Chinese Medicine Prognosis Risk Model Based on a Large-Scale Database After Coronary Revascularization
Visão geral do estudo
Status
Descrição detalhada
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 estudo
Inscrição (Estimado)
Contactos e Locais
Contato de estudo
- Nome: Liu Qiang
- Número de telefone: 13588121905
- E-mail: 19981011@zcmu.com
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Método de amostragem
População do estudo
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
|---|
|
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.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Major Adverse Cardiovascular Events (MACE)
Prazo: 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.
|
12, 24, 36, and 48 weeks post-enrollment
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Traditional Chinese Medicine (TCM) Syndrome Score
Prazo: 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
|
Baseline, 12, 24, 36, 48 weeks post-enrollment
|
|
NYHA Functional Class
Prazo: 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
|
12, 24, 36, 48 weeks post-enrollment
|
|
Multi-omics Biomarkers (exploratory)
Prazo: 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
|
Baseline
|
|
Left Ventricular End-Diastolic Diameter (LVEDD)
Prazo: Baseline
|
Diameter of the left ventricle at end-diastole, measured by echocardiography.
Unit of Measure: mm.
|
Baseline
|
|
Left Ventricular End-Systolic Diameter (LVESD)
Prazo: Baseline
|
Diameter of the left ventricle at end-systole, measured by echocardiography.
Unit of Measure: mm
|
Baseline
|
|
Left Ventricular Posterior Wall Thickness (LVPW)
Prazo: Baseline
|
Thickness of the left ventricular posterior wall in diastole, measured by echocardiography.
Unit of Measure: mm.
|
Baseline
|
|
Interventricular Septal Thickness (IVS)
Prazo: Baseline
|
Thickness of the interventricular septum in diastole, measured by echocardiography.
Unit of Measure: mm
|
Baseline
|
|
Left Ventricular Ejection Fraction (LVEF)
Prazo: Baseline
|
Percentage of blood ejected from the left ventricle per contraction, measured by echocardiography.
Unit of Measure: %.
|
Baseline
|
|
Left Ventricular Fractional Shortening (FS)
Prazo: Baseline
|
Percentage change in left ventricular diameter between diastole and systole, measured by echocardiography.
Unit of Measure: %
|
Baseline
|
|
E/A Ratio
Prazo: Baseline
|
Ratio of early (E) to late (A) ventricular filling velocities, measured by pulsed-wave Doppler echocardiography.
Unit of Measure: ratio
|
Baseline
|
|
Mean Heart Rate (24-hour)
Prazo: Baseline
|
Average heart rate over 24 hours derived from ambulatory electrocardiography (Holter).
Unit of Measure: beats per minute (bpm)
|
Baseline
|
|
Minimum Heart Rate (24-hour)
Prazo: Baseline
|
Lowest heart rate recorded during 24-hour ambulatory ECG, with timestamp.
Unit of Measure: bpm.
|
Baseline
|
|
Maximum Heart Rate (24-hour)
Prazo: Baseline
|
Highest heart rate recorded during 24-hour ambulatory ECG, with timestamp.
Unit of Measure: bpm.
|
Baseline
|
|
Total Premature Ventricular Contractions (PVCs)
Prazo: Baseline
|
Number of premature ventricular contractions recorded over 24 hours by ambulatory ECG.
Unit of Measure: count per 24h
|
Baseline
|
|
Total Premature Atrial Contractions (PACs)
Prazo: Baseline
|
Number of premature atrial contractions recorded over 24 hours by ambulatory ECG.
Unit of Measure: count per 24h
|
Baseline
|
|
Maximum RR Interval
Prazo: Baseline
|
Longest interval between two consecutive R waves on 24-hour ambulatory ECG, indicating cardiac pause.
Unit of Measure: seconds (s)
|
Baseline
|
|
ST Segment Depression Maximum Amplitude
Prazo: Baseline
|
Greatest magnitude of ST segment depression during any ischemic event on 24-hour ambulatory ECG.
Unit of Measure: mm (or mV)
|
Baseline
|
|
ST Segment Depression Longest Duration
Prazo: Baseline
|
Longest duration of a single ST segment depression event on 24-hour ambulatory ECG.
Unit of Measure: minutes (min)
|
Baseline
|
|
SDNN (Heart Rate Variability)
Prazo: 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)
|
Baseline
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- ZSLL-KY-2026-027-01
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .