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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05696379
Other study ID # 2022-0878
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2017
Est. completion date May 31, 2022

Study information

Verified date December 2022
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Coronary microcirculatory dysfunction has been known to be prevalent even after successful revascularization of acute myocardial infarction (AMI) patients, and has been shown to be associated with poor prognosis. Angiography derived index of micro-circulatory resistance (Angio-IMR) is a novel pressure-wire free approach to assess coronary microvascular disease with great diagnostic performance. The current study will further investigate the prognostic value of Angio-IMR in patients with AMI in multicenter retrospective cohort.


Recruitment information / eligibility

Status Completed
Enrollment 5000
Est. completion date May 31, 2022
Est. primary completion date May 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Acute myocardial infarction patients who underwent successful percutaneous coronary intervention Exclusion Criteria: - No appropriate coronary angiography images (inferior image quality, image loss, severe arteries overlap, or significant artifact) - Previous coronary artery bypass graft

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Angiography derived index of micro-circulatory resistance (Angio-IMR)
Angiography derived index of micro-circulatory resistance (Angio-IMR) post percutaneous coronary intervention.

Locations

Country Name City State
China Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang

Sponsors (3)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University RenJi Hospital, Shengjing Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cardiac death or readmission for heart failure in 1 month Incidence of cardiac death or readmission for heart failure during first 1 month follow-up. 1 month
Primary Cardiac death or readmission for heart failure in 6 months Incidence of cardiac death or readmission for heart failure during first 6 months follow-up. 6 month
Primary Cardiac death or readmission for heart failure in 1 year Incidence of cardiac death or readmission for heart failure during first 1 year follow-up. 1 year
Primary Cardiac death or readmission for heart failure in 2 years Incidence of cardiac death or readmission for heart failure during first 2 years follow-up. 2 year
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