CHD - Congenital Heart Disease

6

Review clinical trials related to CHD - Congenital Heart Disease. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Brain Ultrafast Ultrasound Imaging

Congenital heart defects affect 1 in 100 births in France, with rising prevalence due to better care. Despite improved survival, 40% of children post-surgery face neurological impairments, and some of them show brain lesions. Causes include heart defects, genetic syndromes, and surgeries. Some heart defects and support systems increase cerebral risks. Monitoring cerebral perfusion is difficult to assess but emerging ultrafast ultrasound offers real-time, non-invasive blood flow insights.

Participants needed: 300
Trial details
Age: 0-2Biological sex: AllType: ObservationalSponsor: University Hospital, BordeauxUpdated: Dec 23, 2025Locations: 1Duration: 1 Day
Eligibility criteria

Every patient under 2 years old any sex or gender hospitalised in the congenital... [+5]

Anechoic [+1]

Status: Recruiting

Ultrafast Ultrasound Imaging in Pediatric Cardiology

About 13 in 1000 children are born with heart disease. Current tools poorly assess heart filling in children, limiting treatment. This study explores ultrafast ultrasound imaging to measure heart stiffness and perfusion in children with congenital heart disease.

Participants needed: 300
Trial details
Biological sex: AllType: ObservationalSponsor: University Hospital, BordeauxUpdated: Nov 28, 2025Locations: 1Duration: 1 Day
Eligibility criteria

Patients with CHD [+3]

Arrhythmia [+4]

Status: Not yet recruiting

Home-based Cardiovascular Rehabilitation in Young Patients With Congenital Heart Disease: the "Muscle Your Heart" Program

Standard cardiovascular rehabilitation is performed in a medical care and rehabilitation centre. However, it may not be adapted to the patient's profile and there are few medical care and rehabilitation centres specialized in pediatric cardiology. The objective of this study is to evaluate the impact of cardiovascular rehabilitation entirely at home on the physical fitness of young patients with congenital heart disease.

Participants needed: 21
Trial details
Age: 8-25Biological sex: AllType: InterventionalSponsor: University Hospital, BordeauxUpdated: Aug 11, 2025Locations: 1
Eligibility criteria

Indication for home cardiovascular rehabilitation given by the referring cardiol... [+5]

Unstable and/or severe heart failure: severe heart failure (NYHA functional clas... [+21]

Status: Recruiting

NO During CPB in Neonates to Reduce Risk of AKI

Acute kidney injury (AKI) following cardiac surgery for congenital heart defects (CHD) in children affects up to 60% of high risk-patients and is a major cause of both short- and long-term morbidity and mortality. Despite effort, to date, no successful therapeutic agent has gained widespread success in preventing this postoperative decline in renal function. Nitric oxide is an intricate regulator of acute inflammation and coagulation and is a potent vasodilator. The investigators hypothesize that nitric oxide, administered during cardiopulmonary bypass (CPB), may reduce the incidence of AKI.

Participants needed: 40
Trial details
Phase: Phase 3Age: 1-31Biological sex: AllType: InterventionalSponsor: Children's Hospital Medical Center, CincinnatiUpdated: Jul 24, 2025Locations: 1
Eligibility criteria

All neonates (≤31 days) undergoing cardiac surgery with CPB for CHD will be deem...

Failure to obtain informed consent from parent/guardian [+12]

Status: Not yet recruiting

Feasibility of Home Telemonitoring of Infants With Congenital Heart Disease Awaiting Surgery During the First Year of Life

Actually, there is no telemonitoring program that includes newborns or infants with congenital heart disease awaiting cardiac intervention. This is a vulnerable period, prone to clinical complications, rehospitalization, parental stress, and requires monitoring with clinical and therapeutic optimization. The aim of the study is to assess the feasibility and acceptability of monitoring newborns and infants with congenital heart disease awaiting cardiac surgery using the Blue-Line home telemonitoring program.

Participants needed: 20
Trial details
Age: 0-12Biological sex: AllType: InterventionalSponsor: University Hospital, BordeauxUpdated: May 31, 2025Locations: 2
Eligibility criteria

Newborns and/or infants aged 0 to 12 months inclusive at the time of diagnosis. [+4]

Short-term vital prognosis [+6]

Status: Not yet recruiting

Bilateral Ultrasound Guided Superficial Parasternal Intercostal Plane Block Versus Erector Spinae Plane Block

Group (A): This group will receive fentanyl infusion at a dose of (0.5μg/kg/h) all through the whole operation plus ultrasound guided bilateral superficial parasternal intercostal Plane block which will be done by injecting 0.4ml/kg (1:1 solution of bupivacaine 0.25% and lidocaine 1%) at each side3. Group (B): This group will receive fentanyl infusion at a dose of (0.5μg/kg/h) all through the whole operation plus Ultrasound guided bilateral ESPB which will be done by injecting 0.4ml/kg (1:1 solution of bupivacaine 0.25% and lidocaine 1%) at each side .

Participants needed: 50
Trial details
Age: 6-4Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: May 13, 2025Locations: 1
Eligibility criteria

RACHS-1: Categories 1, 2 and 3 [+2]

Patients whose parents or legal guardians refuse to participate. [+5]