Actively Recruiting
Efficacy & Safety of Oral Adjuvants to Phototherapy in Neonatal Hyperbilirubinemia
Led by Amira Adel Fouly · Updated on 2026-03-18
80
Participants Needed
1
Research Sites
95 weeks
Total Duration
On this page
Sponsors
A
Amira Adel Fouly
Lead Sponsor
E
Egyptian Chinese University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Neonatal jaundice, or neonatal hyperbilirubinemia, is a common medical issue in the first two weeks of life, causing prolonged hospitalization and readmissions. It results from elevated total serum bilirubin (TSB) and is manifested as yellowish discoloration of the skin, sclera, and mucous membrane. Clinical jaundice appears in about 60% of term neonates and 80% of preterm infants within the first week of life. Pathologic hyperbilirubinemia occurs when bilirubin levels increase by more than 5 mg/dL/day or 0.2 mg/dL/hour, or when jaundice lasts longer than two to three weeks in full-term infants. In preterm infants, unconjugated hyperbilirubinemia is of particular concern due to their permeable blood-brain barrier and underdeveloped brain. Phototherapy is widely used to reduce or prevent the rise of serum unconjugated bilirubin levels and reduce the need for exchange transfusions. However, phototherapy has both immediate and long-term side effects, and it can only decrease accumulated UCB but does not prevent its accumulation. There is a growing potential to explore novel adjuvant treatments to increase bilirubin clearance, decrease phototherapy duration, and decrease exchange transfusion rate.
CONDITIONS
Official Title
Efficacy & Safety of Oral Adjuvants to Phototherapy in Neonatal Hyperbilirubinemia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Neonates of both genders
- Gestational age of 32 weeks or more
- Ability to tolerate enteral feeding
- Diagnosed with unconjugated non-hemolytic hyperbilirubinemia
- Phototherapy needed within the first week of life
You will not qualify if you...
- Neonates with seizures, hydrops fetalis, hypoxic-ischemic encephalopathy, or major congenital anomalies
- Neonates who had an exchange transfusion within the last 24 hours
- Neonates with hemolytic causes of jaundice such as ABO or Rh incompatibility, or glucose 6-phosphate dehydrogenase deficiency
- Neonates with known hypersensitivity to zinc sulfate or ursodeoxycholic acid
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Neonatal Intensive Care Unit (NICU) of Ain Shams University Hospitals
Cairo, Cairo Governorate, Egypt
Actively Recruiting
Research Team
A
Amira M. Fouly, Demonstrator
CONTACT
D
Dina K. Abou El Fadl, lecturer
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
8
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