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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05967026
Other study ID # 2023PI071
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date July 2023
Est. completion date August 2023

Study information

Verified date July 2023
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this monocentric observationnal study is to describe the characteristics of the myocardial infarction scar in terms of transmurality in residual LVEF>35% patients. The primary objective is to determine the frequency of the criterion "intramural scar ≥1.47cm2" (measured by MRI) in patients who presented with myocardial infarction with residual LVEF≥35%.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 150
Est. completion date August 2023
Est. primary completion date July 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years ; - History of acute coronary syndrome prior to inclusion and having undergone cardiac MRI; - LVEF >35% measured at least 6 weeks post-IDM by echocardiography or MRI; Exclusion Criteria: - Patient with an implantable cardiac device (implantable cardioverter defibrillator or pacemaker) prior to MRI.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU of Nancy Nancy

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intramural scar surface in cm² Intramural scar surface in cm²>1.47cm² 6 weeks after myocardial infarction
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