The main objective of the study is to identify the optimal surgical timing for the treatment of intraventricular defects after acute myocardial infarction.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Patients over eighteen years of age
* Patients with post-myocardial infarction ventricular septal defect treated surgically
* Patients who have signed the informed consent
Exclusion Criteria:
* Patients with post-infarction ventricular septal defect treated with medical/conservative therapy
* Patients with ventricular septal defects not due to acute myocardial infarction
Primary outcome measure(s)
Identify the optimal timing for the surgical intervention. — Possible timing for surgery can be: onset of the infarction episode, hospital admission, before seven days from the acute myocardial infarction or after seven days from the acute myocardial infarction. The optimal timing considering the time interval between the clinical-instrumental diagnosis and the surgical intervention
Trial sites (4)
Facility
City
Region
Status
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna
Bologna
Recruiting
Ospedale Santa Maria della Misericordia Udine
Udine
Udine
Recruiting
Ospedale di Circolo e Fondazione Macchi Varese
Varese
Varese
Recruiting
Hospital Clinic Barcellona
Barcelona
Barcellona
Recruiting
More IRCCS Azienda Ospedaliero-Universitaria di Bologna trials in Italy
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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