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Assessing Neurodevelopment in Congenital Heart Disease. (NEUROHEART)

V

Vall d'Hebron University Hospital (HUVH)

Status

Unknown

Conditions

Congenital Heart Disease

Treatments

Procedure: Sonography
Procedure: Surgical intervention
Procedure: cord blood sample
Device: Magnetic Resonance Imaging
Procedure: Brain monitoring
Other: Bailey Test

Study type

Interventional

Funder types

Other

Identifiers

NCT02996630
PR(AMI)317/2012

Details and patient eligibility

About

Congenital heart disease (CHD) is the most prevalent congenital malformation affecting 1 in 100 newborns per year. Children with CHD are a known risk population for brain injury, with neurodevelopmental alterations shown over time in up to 50% of cases. No adequate description exists of the type of neurocognitive anomalies or risk factors associated with CHD, and consequently no prognostic markers that may allow identification of high-risk cases are available.

Full description

The main objectives of this study are: 1. to describe the neurodevelopmental outcome of patients with CHD at 24 months of age; 2. identify the subgroup with poorer outcome; and 3. evaluate the utility of fetal and postnatal diagnostic techniques for early detection of patients at risk for altered neurological outcomes.

Seven Spanish referral centers for CHD included in the research network on maternal and child health currently participating in this prospective multicentric case-control coordinated study. Fetuses with CHD (transposition of great arteries, tetralogy of Fallot, hypoplastic left heart syndrome and septal defects) will be studied from 24 weeks of gestation to 2 years of age. Diagnostic tests will be repeated throughout the study in all patients, from the fetal period to 24 months of age, and will include: fetal cerebral hemodynamic Doppler assessment, functional echocardiography, brain MRI, regional cerebral oxymetry, electroencephalography and serum neurological and cardiac biomarkers analysis. Neurodevelopmental assessment will be made at 12 months of age using the ages and stages questionnaire (ASQ) and at 24 months of age with the Bayley-III test. From this data, statistical analysis will select the most useful as predictors of damage; to be then combined and create algorithms for predicting brain damage and poor neurodevelopment. Once description has been made, we will proceed to identify amongst our results, children with the poorest neurological outcome and remark possible common prenatal and early life markers in them as well as the CHD severity they present.

While advances in early diagnosis and postnatal management have increased survival in CHD children, worrying long-term outcomes, particularly neurodevelopmental disability, have emerged as a key prognostic factor in the counseling of these pregnancies. Evidence available does not allow clinicians to assess on neurological prognosis although has opened up the possibility of finding prenatal markers of brain damage. Even though, no prospective studies have been performed until now. We present a multicentric prospective study able to recruit enough fetal CHD affected pregnancies to obtain neurological prognostic tools.

Enrollment

250 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Single pregnancies
  • Major Congenital Heart Disease
  • Informed Consent Signed

Exclusion criteria

  • Major extra-cardiac malformations
  • Parental Refusal to participate
  • Maternal Chronic Disease
  • Multiple Pregnancies

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

250 participants in 2 patient groups

Healthy fetuses
Other group
Description:
Pregnant patients carrying a healthy fetus. Interventions in this group will be: cord blood sample, sonography, Magnetic Resonance Imaging and bailey test.
Treatment:
Procedure: cord blood sample
Device: Magnetic Resonance Imaging
Procedure: Sonography
Other: Bailey Test
Congenital Hearth Disease
Other group
Description:
Pregnant patients carrying a fetus with a moderate-severe congenital heart disease Interventions in this group will be: cord blood sample, sonography, Magnetic Resonance Imaging, Surgical intervention, brain monitoring and bailey test.
Treatment:
Procedure: cord blood sample
Device: Magnetic Resonance Imaging
Procedure: Sonography
Procedure: Surgical intervention
Other: Bailey Test
Procedure: Brain monitoring

Trial contacts and locations

1

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Central trial contact

Aina Ruiz, MD; Irene Ribera, MD

Data sourced from clinicaltrials.gov

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