Altered Cerebral Growth and Development in Infants With Congenital Heart Disease
NCT04233775 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 60
Last updated 2023-07-19
Summary
Background: Congenital heart disease (CHD) is the most frequent inborn defect with an incidence of 1 in 100 newborns per year, i.e. 800 children born in Switzerland per year. 10% to 15% of cases are born with single ventricle (SV), the most complex type of CHF requiring immediate surgical intervention after birth. Infants with SV CHD are treated in three surgical staged procedures over the first three years of life. However, cerebral injuries occur in around 40% of those children and impact neurocognitive abilities. As more than 90% of all infants with CHD survive to adulthood, scientific concern is focussed on patient-individual course brain growth and development within the relative contribution of fetal, perinatal, cardiac and surgical risk factors. Therefore, serial cerebral MRI examinations are needed, starting (1) at the third trimester during fetal life proceeding to (2) pre- and postoperative time points at the stage I surgery after birth and (3) before stage II surgery at 4 months of age. We will compare the cerebral MRI findings with a healthy control population, recruited at the same time points, and correlate brain growth and development with the neurodevelopmental outcome assessed at one year of age. Three Pediatric Heart Centers in Switzerland and Germany will participate.
The overall aims are:
1. To analyse the patient-individual cerebral developmental trajectories, brain growth and determine the time course of brain abnormalities in infants with single ventricle CHD by serial cerebral MRI during fetal life, after birth and at an age of 4 months (primary endpoints).
2. To determine the neurodevelopmental outcome at one year of age using the Bayley III and will be correlated with the brain growth and brain development in the third trimester of fetal life and at the age of 4 months (secondary endpoints).
3. To analyse fetal, neonatal, surgery-related and intensive care associated factors determining the patient-individual course for altered cerebral growth and impaired neurodevelopmental outcome at one year of age.
Methodology: We will prospectively enroll fetuses and neonates with single ventricle CHD at the three Pediatric Heart Centers in Switzerland (Zurich, Bern) and Germany (Giessen). Advanced MR imaging will assess cerebral volumes, microstructural and hemodynamic changes at repeated time points during the third trimester of fetal life (32. week of gestation), the perioperative neonatal period before and after stage I surgery and before stage II surgery at 4 months of age. Biomechanical analysis of longitudinal changes of brain morphology will be applied to longitudinal fetal and neonatal MRI data. Outcome is determined with the Bayley-III at one year of age.
Significance: Using a population-based sample of children with single ventricle CHD, we will be able to determine cerebral growth from the third fetal trimester until the first 4 months after birth, when the brain is most rapidly growing. By performing serial brain imaging, the knowledge of etiological pattern affecting cerebral growth, development and brain injury will increase. Morphometric and biomechanical analysis of brain growth patterns will be performed that may capture fine-grained changes associated with CHD. By correlating these data with the neurodevelopmental outcome at one year of age it will be possible to identify specific risk constellations leading to impaired brain development and categories of brain injuries that confer a higher risk of adverse outcome. The better understanding of the pathophysiological mechanisms will serve as the basis for neuroprotective studies and pharmacological trials aiming to improve outcomes in children with CHD in the future.
Conditions
- Neurodevelopmental Disorders
- Congenital Heart Disease
- Brain Injuries
- Fetal Growth Retardation
Sponsors & Collaborators
-
University Children's Hospital, Zurich
lead OTHER
Principal Investigators
-
Walter H Knirsch, MD · University Children's Hospital, Pediatric Heart Center, Pediatric Cardiology
Eligibility
- Min Age
- 0 Days
- Max Age
- 6 Months
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-01-01
- Primary Completion
- 2023-12-31
- Completion
- 2024-12-31
Countries
- Switzerland
Study Locations
More Related Trials
-
Functional Muscle Characteristics and Cardio-respiratory Interaction in Patients With Fontan Palliation
NCT04151004 ·Status: COMPLETED ·Phase: NA
-
Heart Failure in Adult Patients With a History of Congenital Heart Disease
NCT00208754 ·Status: TERMINATED
-
Transcoronary Infusion of Cardiac Progenitor Cells in Patients With Single Ventricle Physiology
NCT01273857 ·Status: COMPLETED ·Phase: PHASE1
-
Validation of Cardiac Magnetic Resonance Sequences in Patients With Single Ventricles
NCT04017494 ·Status: UNKNOWN
-
Cerebrum and Cardiac Protection With Allopurinol in Neonates With Critical Congenital Heart Disease Requiring Cardiac Surgery With Cardiopulmonary Bypass
NCT04217421 ·Status: RECRUITING ·Phase: PHASE3
-
Congenital Heart Disease GEnetic NEtwork Study (CHD GENES)
NCT01196182 ·Status: ACTIVE_NOT_RECRUITING
-
Study of Intramyocardial Injection of Ventrix Bio Extracellular Matrix (VentriGel) to Assess the Safety and Feasibility in Pediatric Patients with Hypoplastic Left Heart Syndrome (HLHS)
NCT06461676 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1
-
Nutritional Failure in Infants With Single Ventricle Congenital Heart Disease
NCT01821287 ·Status: COMPLETED
-
Maternal Hyperoxygenation in Fetal Left Heart Hypoplasia
NCT05334966 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Isolated Mild Fetal Ventriculomegaly and Neurodevelopmental Outcome
NCT00256906 ·Status: TERMINATED
-
National Collaborative to Improve Care of Children With Complex Congenital Heart Disease
NCT02852031 ·Status: RECRUITING
-
PRecIsion Medicine in CardiomyopathY
NCT04036799 ·Status: ACTIVE_NOT_RECRUITING
-
Molecular Basis of Congenital Heart Defects
NCT00579358 ·Status: WITHDRAWN
-
Single Ventricle Outcome
NCT00308217 ·Status: COMPLETED
-
An Evaluation of Routine Developmental Follow-Up in Infants and Children With Congenital Heart Disease
NCT01567579 ·Status: COMPLETED
-
Molecular and Cellular Characterization of Cardiac Tissue in Postnatal Development
NCT00243776 ·Status: RECRUITING
-
Cardiac Displacement From Third Trimester to Early Childhood
NCT02583763 ·Status: ACTIVE_NOT_RECRUITING
-
Fetal Aortic Valvuloplasty for Evolving Hypoplastic Left Heart Syndrome
NCT06342999 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Long-term Outcomes of Children With Hypoplastic Left Heart Syndrome and the Impact of Norwood Shunt Type
NCT02455531 ·Status: ACTIVE_NOT_RECRUITING
-
Fetal Intervention for Aortic Stenosis and Evolving Hypoplastic Left Heart Syndrome
NCT01736956 ·Status: COMPLETED ·Phase: NA
-
Influence of Genetic Polymorphisms on Ventricular Structure and Function in Patients With Single Ventricle Anatomy
NCT00165984 ·Status: COMPLETED
-
Cerebral Blood Flow in Single Ventricles Throughout Staged Surgical Reconstruction
NCT02135081 ·Status: COMPLETED
-
Study of Energy Expenditure in Infants With Ventricular Septal Defects
NCT00006272 ·Status: UNKNOWN
-
Accelerated Aging in Newborns and Adults With Congenital Heart Disease
NCT05667870 ·Status: UNKNOWN
-
Death Following Congenital Heart Surgery
NCT00215072 ·Status: TERMINATED