- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07613060
Establishment of Disease Characteristics and a Chinese Medicine Prognosis Risk Model Based on a Large-Scale Database After Coronary Revascularization
연구 개요
상세 설명
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.
연구 유형
등록 (추정된)
연락처 및 위치
연구 연락처
- 이름: Liu Qiang
- 전화번호: 13588121905
- 이메일: 19981011@zcmu.com
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
|---|
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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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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Major Adverse Cardiovascular Events (MACE)
기간: 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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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Traditional Chinese Medicine (TCM) Syndrome Score
기간: 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
기간: 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)
기간: 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)
기간: 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)
기간: Baseline
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Diameter of the left ventricle at end-systole, measured by echocardiography.
Unit of Measure: mm
|
Baseline
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Left Ventricular Posterior Wall Thickness (LVPW)
기간: 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)
기간: 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)
기간: 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)
기간: Baseline
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Percentage change in left ventricular diameter between diastole and systole, measured by echocardiography.
Unit of Measure: %
|
Baseline
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E/A Ratio
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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)
기간: 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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공동 작업자 및 조사자
스폰서
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- ZSLL-KY-2026-027-01
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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