Actively Recruiting
Prognosis in Adult Patients With Congenital Heart Disease
Led by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Updated on 2024-12-09
450
Participants Needed
1
Research Sites
249 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a mono-center observational ambispective study in which adult patients with congenital heart disease evaluated at our institution will be enrolled. The primary endopoint is to assess the clinical and echocardiographic predictors of adverse events during follow-up (death, arrhythmias, cardiac hospitalization). The secondary endpoints are: 1) evaluation of the incidence of the singular components of the primary endpoint; 2) evaluation of the prognostic impact of acquired lesions, including valve disease not present at birth; 3) need for surgical/percutaneous interventions during follow up. Participants will be evaluated in the context of scheduled follow-up visits in our Outpatient ACHD Clinic. No interventions/drug administration will be performed other than those required by standard clinical practice.
CONDITIONS
Official Title
Prognosis in Adult Patients With Congenital Heart Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients evaluated in our ACHD Outpatient Clinic between January 2014 and December 2026
- Age 63 18 years
You will not qualify if you...
- Patients without congenital heart disease confirmed during the first evaluation
- Impossibility to retrieve information about the first clinical evaluation in our clinic from our electonic datasets
- Follow up shorter than one-year
- Refused consent to participate to the study.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Fondazione Policlinico Universitario Agostino Gemelli
Rome, RM, Italy, 00168
Actively Recruiting
Research Team
F
Francesca Graziani, MD, PhD
CONTACT
G
Giulia Iannaccone, 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
1
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