Actively Recruiting

Age: 18Years +
All Genders
NCT04050956

French Cohort of Myocardial Infarction Evaluation

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-06-25

30000

Participants Needed

1

Research Sites

1567 weeks

Total Duration

On this page

Sponsors

A

Assistance Publique - Hôpitaux de Paris

Lead Sponsor

N

Novartis

Collaborating Sponsor

AI-Summary

What this Trial Is About

Over the last two decades, considerable progress has been made in the management of Acute Myocardial Infarction (AMI), both in the acute phase and in monitoring beyond the hospital phase. Nevertheless, the evolution of care practices and their impact on the mid- and long-term prognosis of patients admitted to the intensive care unit for acute myocardial infarction remain relatively little studied exhaustively. The aim of this study is to assess the profile of AMI patients, their management and follow-up in order to evaluate the relationship between these factors and outcomes.

CONDITIONS

Official Title

French Cohort of Myocardial Infarction Evaluation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Myocardial infarction within 48 hours of symptom onset, confirmed by increased or falling troponin or CPKMB with at least one of the following: symptoms of myocardial ischemia, pathological Q waves, or ST-T changes compatible with ischemia
  • Written consent to participate
  • Covered by French medical insurance (S�curit� Sociale)
Not Eligible

You will not qualify if you...

  • Heart attack caused by a medical procedure within 48 hours prior to admission
  • Diagnosis of acute myocardial infarction ruled out in favor of another condition

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hôpital Bichat, AP-HP

Paris, France, 75018

Actively Recruiting

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Research Team

T

Tabassome SIMON

CONTACT

P

Philippe Gabriel STEG

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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