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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02786654
Other study ID # PG/13/81/30474BB
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2007
Est. completion date June 2013

Study information

Verified date June 2019
Source University of Leeds
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The aim of the study is to investigate the association between the use of β blockers and mortality among hospital survivors of acute myocardial infarction without heart failure.


Recruitment information / eligibility

Status Completed
Enrollment 179810
Est. completion date June 2013
Est. primary completion date June 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- acute myocardial infarction patients only

- aged 18 to 100 years

Exclusion Criteria:

- other final diagnosis besides acute myocardial infarction

- died in-hospital

- patients with missing mortality data

- aged > 100

- patients with previous acute myocardial infarction or angina

- patients who have received coronary interventions before

- patients with heart failure

- patients with ß blocker prior use

- patients contraindicated for ß blocker use

- patients with use of a loop diuretic

Study Design


Locations

Country Name City State
United Kingdom University of Leeds Leeds

Sponsors (1)

Lead Sponsor Collaborator
University of Leeds

Country where clinical trial is conducted

United Kingdom, 

References & Publications (1)

Dondo TB, Hall M, West RM, Jernberg T, Lindahl B, Bueno H, Danchin N, Deanfield JE, Hemingway H, Fox KAA, Timmis AD, Gale CP. ß-Blockers and Mortality After Acute Myocardial Infarction in Patients Without Heart Failure or Ventricular Dysfunction. J Am Coll Cardiol. 2017 Jun 6;69(22):2710-2720. doi: 10.1016/j.jacc.2017.03.578. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary All cause mortality 1 year
Secondary All cause mortality 6 months
Secondary All cause mortality 30 days
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