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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05653765
Other study ID # HenanICE202201
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 20, 2022
Est. completion date March 20, 2024

Study information

Verified date November 2023
Source Henan Institute of Cardiovascular Epidemiology
Contact Quan Guo, MD
Phone +8615670510031
Email xinyiguoquan@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to learn about in STEMI with Primary PCI Patients. The main questions it aims to answer are: - To determine the value of AMR in predicting the long-term clinical prognosis of patients with STEMI after PPCI, and to find the best cut-off value. - Analyze the factors of PPCI affecting AMR and explore the effective measures of PPCI microcirculation protection. Radiographic images of STEMI receiving primary PCI treatment in several chest pain centers in China will be included. The last image of the infarct-related vessel will be used as a target to calculate its AMR. The relationship between AMR and long-term clinical prognosis was analyzed.


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date March 20, 2024
Est. primary completion date December 20, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Aged 18 or older - Type 1 myocardial infarction - Receive PPCI Exclusion Criteria: - Failed to identify culprit vessels. - Structural heart disease with moderate to severe aortic valve or mitral regurgitation and or stenosis that may affect cardiac function - Dialysis patients with severe renal insufficiency - Severe and uncontrollable arrhythmia - Complicated with dilated cardiomyopathy - Unable to tolerate dual antiplatelet therapy - Severe and uncontrollable anemia - Hyperthyroidism - TIMI blood flow 0-1 grade after PPCI

Study Design


Locations

Country Name City State
China Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Shanghai
China Shangqiu first people's Hospital Shangqiu Henan
China Department of Cardiology, First Affiliated Hospital of Xinxiang Medical University Xinxiang Henan
China Fuwai central China cardiovascular Hospital Zhengzhou Henan

Sponsors (1)

Lead Sponsor Collaborator
Henan Institute of Cardiovascular Epidemiology

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary MACEs cardiac death, hospitalization for heart failure, target vessel revascularization,non-fatal MI 12 months
Secondary cardiac death Rates of individual components of MACE 12 months
Secondary hospitalization for heart failure Rates of individual components of MACE 12 months
Secondary target vessel revascularization Rates of individual components of MACE 12 months
Secondary non-fatal MI Rates of individual components of MACE 12 months
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