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Starting soon Not applicable

Prevalence of Liver Dysfunction in Pediatric Patients With Congenital Heart Disease at Assiut.

NCT07144501 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-09-15
Last updated
2025-08-27

Condition(s) studied

Congenital Heart DiseaseLiver Dysfunction

Investigational drug(s) / intervention(s)

UltrasonographyBlood Sampling

Ultrasonography: Ultrasound, also known as sonography or ultrasonography, is a medical imaging technique that uses high-frequency sound waves to create real-time images of internal body structures

Blood Sampling: To assess hepatic function in congenital heart disease (CHD) patients, blood samples will be collected from all patients in our study for: * Alanine Transferase (ALT). * Aspartate Aminotransferase (AST). * Gamma Glutamyl Transferase (GGT). * Alkaline Phosphatase (ALP). * Total/direct bilirubin. * Albumin. * Prothrombin time. * International Normalized Ratio (INR). * Platelet count.

Study summary

Liver dysfunction is a well-documented complication in patients with congenital heart disease (CHD). The mechanisms leading to hepatic dysfunction may be multifactorial. Key risk factors for liver dysfunction in CHD include prolonged hypoxemia, high venous pressure, and prolonged duration of heart disease.

While global studies have extensively explored this association, the prevalence of liver dysfunction in CHD varies, with studies reporting hepatic fibrosis in 30-40% of Fontan patients, while regional data, particularly from Egypt, remain limited.

In this research we aim to determine the prevalence of biochemical and radiological hepatic abnormalities in pediatric CHD patients attending Assiut University Children's Hospital.

Eligibility

Sex
ALL
Min age
—
Max age
16 Years
Healthy volunteers
No
Inclusion Criteria: * Confirmed pediatric CHD patients attending Assiut University Children's Hospital. * Age: from birth up to 16 years old. Exclusion Criteria: * Patients with primary liver disease. * Recent cardiac surgery (\<3 m) (to exclude acute postoperative liver injury). * Active systemic infection/sepsis (to avoid confounding liver enzyme elevations).

Primary outcome measure(s)

  • To assess the prevalence of hepatic dysfunction among CHD — 5 months
    To assess the prevalence of hepatic dysfunction among CHD patients attending Assiut University Children's Hospital

Trial sites (1)

FacilityCityRegionStatus
Assiut University Children Hospital. Asyut Assiut City
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 NCT07144501 on ClinicalTrials.gov ↗ ← All trials in Egypt