Actively Recruiting

Age: 18Years +
All Genders
NCT06799780

Study on Post-acute Myocardial Infarction Ventricular Defect: Outcome Evalutation in Relation to Surgical Timing

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-29

100

Participants Needed

4

Research Sites

146 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main objective of the study is to identify the optimal surgical timing for the treatment of intraventricular defects after acute myocardial infarction.

CONDITIONS

Official Title

Study on Post-acute Myocardial Infarction Ventricular Defect: Outcome Evalutation in Relation to Surgical Timing

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over eighteen years of age
  • Patients with post-myocardial infarction ventricular septal defect treated surgically
  • Patients who have signed the informed consent
Not Eligible

You will not qualify if you...

  • Patients with post-infarction ventricular septal defect treated with medical/conservative therapy
  • Patients with ventricular septal defects not due to acute myocardial infarction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Bologna, Bologna, Italy, 40138

Actively Recruiting

2

Ospedale Santa Maria della Misericordia Udine

Udine, Udine, Italy, 33100

Actively Recruiting

3

Ospedale di Circolo e Fondazione Macchi Varese

Varese, Varese, Italy, 21010

Actively Recruiting

4

Hospital Clinic Barcellona

Barcelona, Barcellona, Spain, 08024

Actively Recruiting

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Research Team

L

Luca Di Marco, MD

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

0

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