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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06335901
Other study ID # xx20190901
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2020
Est. completion date April 30, 2022

Study information

Verified date March 2024
Source Xinjiang Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluated and compared the prognostic value of different Baseline data and clinical variables to develop a risk ractor ediction model in patients with CHD.


Recruitment information / eligibility

Status Completed
Enrollment 20000
Est. completion date April 30, 2022
Est. primary completion date January 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 79 Years
Eligibility Inclusion Criteria 1. Patients diagnosed with Coronary Heart Disease (CHD) admitted to The First Affiliated Hospital of Xinjiang Medical University. The diagnosis is based on clinical assessments, including symptomatic evaluation, electrocardiographic findings, and coronary imaging studies. Exclusion Criteria 1. Patients who have experienced a Myocardial Infarction (MI) within the last month. 2. Patients who have undergone coronary revascularization, such as coronary artery bypass grafting (CABG) or percutaneous coronary intervention (PCI), in the last three months. 3. Patients with a pre-planned coronary revascularization procedure.

Study Design


Intervention

Drug:
Drug:Standard therapy
Percutaneous coronary Intervention

Locations

Country Name City State
China The First Affiliated Hospital of Xinjiang Medical University Ürümqi Xinjiang

Sponsors (1)

Lead Sponsor Collaborator
Xinjiang Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Death (All-cause mortality?Cardiac mortality ) 5 years of follow-up deaths occurred during this period
Secondary Major adverse cardiovascular events 5 years of follow-up deaths occurred during this period
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