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NCT04564365 Clinical Trial

The Contemporary Role of Beta Blockers in Patients With Acute Myocardial Infarction

Acute Coronary Syndrome Clinical Trial

Official title:
Influence of Beta-Blockers on Prognosis in Patients With Acute Myocardial Infarction Complicated With Normal Ejection Fraction

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04564365
Other study ID # 2020-09-22
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 30, 2019
Est. completion date December 25, 2021

Study information
Verified date June 2021
Source Chongqing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The use of beta blockers after acute myocardial infarction is a core component of drug therapy, but evidence is primarily derived from patients who did not receive reperfusion therapy and secondary prophylaxis.In contemporary times, the prognostic value of beta blockers in patients with acute myocardial infarction has been questioned, particularly in patients without reduced heart failure/ejection fraction after acute myocardial infarction.

Recruitment information / eligibility
Status Recruiting
Enrollment 1000
Est. completion date December 25, 2021
Est. primary completion date November 25, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - The diagnosis of acute myocardial infarction was clear and the left ventricular ejection fraction was normal Exclusion Criteria: - History of heart failure Died in hospital

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• beta-blocker
To investigate the relationship between the use of beta blockers and prognosis in patients with normal ejection fraction after acute myocardial infarction

Locations
Country Name City State
China The first affiliated Hospital of Chongqing Medical University Chongqing

Sponsors (1)
Lead Sponsor Collaborator
Chongqing Medical University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary mortality all-cause mortality the median time of 8 months
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