Actively Recruiting

Phase 4
Age: 1Day - 1Month
All Genders
NCT06517862

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

Age: 1Day - 1Month
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Neonatal Intensive Care Unit (NICU) of Ain Shams University Hospitals

Cairo, Cairo Governorate, Egypt

Actively Recruiting

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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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Efficacy & Safety of Oral Adjuvants to Phototherapy in Neonatal Hyperbilirubinemia | DecenTrialz