Ireland
--:--IST
Recruiting Observational

Follow-up of a Cohort of Patients With Aortic Valve Bicuspidia

NCT03139786 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2010-09-16
Last updated
2026-06-15

Condition(s) studied

Aortic Valve, Bicuspid

Investigational drug(s) / intervention(s)

Study the natural history of bicuspid

Study the natural history of bicuspid: Study the natural history of bicuspid

Study summary

The aortic valve bicuspidia (BVA) is a congenital condition corresponding to the presence of 2 sigmoids instead of 3. This is the most common cardiac congenital anomaly affecting 0.5 to 2% of the population The general rule. BVA may be associated with structural damage to the ascending aorta, which exposes BVA patients to a risk of developing ascending aortic aneurysm and acute aortic accidents. Recent data from the literature have revealed that the natural history of BVA is marked by a possible development towards significant valvulopathy and / or an ascending aortic aneurysm often requiring surgical treatment. However, the natural history of bicuspid disease remains poorly understood and the prognostic factors for progression to severe valvulopathy and / or aneurysmal dilatation of the ascending aorta remain to be determined.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * All patients examined in the echocardiography laboratory whose objective examination was a bicuspid valve of the aortic valve * Bicuspidia may be formerly known Exclusion Criteria: * Refusal to participate * Patients who had already undergone bicuspid surgery or ascending aorta before being examined at the echocardiography laboratory

Primary outcome measure(s)

  • Analysis of 10 year mortality in cardiac surgery in a patient with bicuspid — 10 years
    Analyzing the natural history of Bicuspidia

Trial sites (1)

FacilityCityRegionStatus
CHU Amiens Picardie Amiens Picardie Recruiting
Official registry record

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.

View NCT03139786 on ClinicalTrials.gov ↗ ← All trials in France