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Study identifier: NCT06517862 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy & Safety of Oral Adjuvants to Phototherapy in Neonatal Hyperbilirubinemia

Condition: Neonatal Hyperbilirubinemia  ·  Sponsor: Amira Adel Fouly

PhasePhase 4
Planned participants80
Who can joinAll sexes, 1 Day to 1 Month
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Amira M. Fouly, Demonstrator  ·  +20 102 303 3092  ·  amira.mohamed@ecu.edu.eg

Dina K. Abou El Fadl, lecturer  ·  +20 100 544 2855  ·  Dkhaled@fue.edu.eg

Always discuss trial participation with your own doctor first.

Locations (1)

Neonatal Intensive Care Unit (NICU) of Ain Shams University HospitalsCairo, Cairo Governorate, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT06517862