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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06799780
Enrollment
100
Registered
2025-01-29
Start date
2024-02-12
Completion date
2026-11-30
Last updated
2025-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Disease, Myocardial Infarction (MI)

Brief summary

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

Detailed description

Identify the optimal timing for the treatment of post-infarction ventricular defect, considering the time interval between the clinical-instrumental diagnosis and the surgical intervention.

Interventions

None listed

Sponsors

IRCCS Azienda Ospedaliero-Universitaria di Bologna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
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

Countries

Italy, Spain

Contacts

Primary ContactLuca Di Marco, MD
luca.dimarco@aosp.bo.it0512149044

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026