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NCT05719545 Clinical Trial

A Cohort of Patients Undergoing Percutaneous Coronary Intervention

Myocardial Infarction Clinical Trial

— APCIcohort  

Official title:
A Longitudinal Cohort of Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05719545
Other study ID # 2021-206-02
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 1, 2021
Est. completion date December 30, 2026

Study information
Verified date January 2023
Source Jinan Central Hospital
Contact Guohai Su, doctor
Phone +86-18854125717
Email huangrong9277@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To investigate the risk factors involved in the occurrence and prognosis of the patients with acute coronary syndrome, patients undergoing percutaneous coronary intervention will be recruited and followed up for at least 2 years.

Description:

Patients with acute coronary syndrome undergoing percutaneous coronary intervention will be recruited and prospectively followed up for the incidence of major adverse cardiovascular events (MACE events), including all-cause mortality, cardiovascular mortality, ischemic stroke. Blood and fecal samples will be collected for further analysis. The basic and clinical information will be collected such as diagnosis, medical history, laboratory test results, therapy methods, prognosis and follow-up information. The risk factors involved in the occurrence and prognosis of acute coronary syndrome will be investigated.

Recruitment information / eligibility
Status Recruiting
Enrollment 10000
Est. completion date December 30, 2026
Est. primary completion date December 30, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Diagnosed as acute coronary syndrome and needed to undergo percutaneous coronary intervention. - >18 years old. Exclusion Criteria: - With malignant tumors, acute infectious diseases and advanced liver diseases. - Won't sign an inform consent.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China Jinan Central Hospital Jinan Shandong

Sponsors (2)
Lead Sponsor Collaborator
Su Guohai Shandong First Medical University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary major adverse cardiovascular events all-cause mortality, cardiovascular mortality, ischemic stroke 2-year outcome and long-term outcome
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