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Clinical Trials/NCT05159791
NCT05159791
Completed
Not Applicable

New Patient-specific Functional Assessment of the Anomalous Aortic Origin of Coronary Arteries.

IRCCS Policlinico S. Donato1 site in 1 country60 target enrollmentNovember 23, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
IRCCS Policlinico S. Donato
Enrollment
60
Locations
1
Primary Endpoint
Identification of myocardial ischemia on simulation model
Status
Completed
Last Updated
last year

Overview

Brief Summary

Anomalous Aortic Origin of the Coronary Arteries (AAOCA) is a rare congenital disease that may cause sudden death in young subjects. Frequently the first and only presentation is with an acute event (such as myocardial infarction or sudden cardiac deaths) during physical effort. Not only symptoms are often absent, but also provocative tests fail to induce ischemia or related signs, showing in most patients negative results. For these limitations, the decision to undergo corrective surgery is based on the morphologic characteristics without the support of a functional evaluation. The study focused on developing a personalized ischemic risk assessment with the aid of fluid dynamic simulations. The simulation system integrate clinical data from different diagnostic sources and integrate them with coronary blood flow evaluation at rest and during simulated physical effort.

Detailed Description

Anomalous Aortic Origin of Coronary Arteries (AAOCA) is a congenital condition where one or more coronary vessels originate from an ectopic site within the aorta, such as the opposite or wrong sinus of Valsalva. Its prevalence in the general population, has been estimated between 0.03% and 0.23% depending on the variant evaluated. The anomalous left or right coronary artery, besides its origin, may take 5 different general courses: interarterial, prepulmonic, subpulmonic, retroaortic or retrocardiac. Each of these forms may be subject to cause myocardial ischemia and subsequent sudden death during physical and sport activity. In most cases, the disease is silent and does not show any symptoms before the sudden cardiac death event (SCD). Only a few AAOCA subjects report symptoms before SCD that usually occurs unexpectedly after a moderate or intense physical activity. It is extremely hard to study the causing factors in a clinical environment due to the stochastic nature of the myocardial ischemic event and the inability to reproduce the exact effort conditions. Even when a complete assessment is performed, there is no clinical exam that can reproduce sustained exercise conditions responsible for triggering ischemia and SCD. Even if such an exam would exist and provide adequate results, the risk of SCD exceeds the benefits of having a correct diagnosis. To overcome all the current diagnostic limitations the ideal diagnostic test has to investigate coronary blood supply, myocardial oxygen demand in relation to the physical activity (intensity and duration) required for triggering an ischemic event, without putting the subjects at risk. To date the only possible way to reproduce such conditions is a subject-specific virtual simulation of aortic root and coronary artery integrated with coronary blood flow simulation able to mimic pressure, flow, and oxygen demand characteristics similar to those of intense exercise, in relation to changes that anomalous coronary undergoes under such conditions.

Registry
clinicaltrials.gov
Start Date
November 23, 2021
End Date
December 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
IRCCS Policlinico S. Donato
Responsible Party
Principal Investigator
Principal Investigator

Mauro Lo Rito

Pediatric Cardiac Surgeon and Research Associate

IRCCS Policlinico S. Donato

Eligibility Criteria

Inclusion Criteria

  • Patients with a diagnosis of AAOCA of any age will undergo fluid dynamic simulation
  • Patients with age \> 14 with diagnosis of AAOCA will undergo to invasive coronary flow measurements
  • Informed consent

Exclusion Criteria

  • A presence of major associated congenital heart anomalies
  • Contraindication to the execution of the diagnostic examination requested such as age \< 14 years for invasive coronary flow measurements

Outcomes

Primary Outcomes

Identification of myocardial ischemia on simulation model

Time Frame: 3 years

Assess myocardial ischemia in the patient's specific model during simulated effort correlating coronary artery blood supply to myocardial oxygen demand.

Secondary Outcomes

  • Invasive coronary flow distribution assessment(During clinical diagnostic evaluation, average 3 months after)
  • In vitro effort fluid dynamic simulation(3 years)
  • Integration of different coronary artery imaging modality(During clinical diagnostic evaluation, average 6 months)
  • Computational fluid dynamic simulation(3 years)

Study Sites (1)

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