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Study identifier: NCT07095829 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prognostic Model of Postnatal Circulation in Pulmonary Atresia-critical Stenosis With Intact Ventricular Septum

Condition: Pulmonary Atresia With Intact Ventricular Septum · Congenital Heart Disease · Fetal Cardiac Disorder  ·  Sponsor: Hospital Universitario 12 de Octubre

PhaseN/A
Planned participants150
Who can joinAll sexes, 16 Weeks to 28 Weeks
Healthy volunteersNo

About this study

Pulmonary atresia (PA)/critical stenosis (CS) with intact ventricular septum (PA/CS-IVS) is a rare congenital heart disease (CHD), that presents heterogeneously. Prognosis is conditioned by the possibility of achieving a primary repair with biventricular circulation (BV) or a one-and-a-half ventricle solution vs. a palliative approach bound to a univentricular (UV) circulation in which both survival and quality of life are significantly impaired. Predicting UV circulation prenatally is still a challenge. The aim of this study is: 1/ to evaluate the natural history of the disease and develop a prognostic model for the prediction of transplantation-free survival with a biventricular or a one-and-a-half repair at 2 years postnatal age 2/ To develop a model to predict the risk of right ventricle dependent coronary circulation 3/ To evaluate prenatal and postnatal outcomes in non-intervened fetuses with a confirmed postnatal diagnosis of PA-CS/IVS including Intrauterine death, neonatal/Infant death, number of required postnatal procedures, need for oxygen support, need for cardiac transplantation

This description comes directly from the study's public registry record.

Talk to the study team

Cecilia Villalain, MD PhD  ·  +34913908310  ·  cecilia.villalain@salud.madrid.org

Alberto Galindo, MD PhD  ·  +34913908310  ·  agalindo@salud.madrid.org

Always discuss trial participation with your own doctor first.

Locations (2)

Hospital Universitario 12 de OctubreMadrid, SpainRecruiting
University of GothenburgGothenburg, SwedenActive Not Recruiting

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Source record: clinicaltrials.gov/study/NCT07095829