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Clinical Trials/IRCT20190708044158N1
IRCT20190708044158N1CompletedPhase 3

Comparison between the Effect of Fenofibrate and Clofibrate on Term Neonates with Hyperbilirubinemia

Babol University of Medical Sciences0 sites80 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
80

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
3 days to 28 days (—)
Sex
All

Inclusion Criteria

  • Term neonates(37 weeks to 41 weeks and 6 days) that their ages are more than 72 hours.
  • They were admitted for jaundice, total bilirubin serum more than 15 mg/dl.
  • They were otherwise healthy.
  • They did not receive therapy other than phototherapy.

Exclusion Criteria

  • Premature neonates
  • IUGR infants
  • Neonates with congenital anomaly
  • Neonates with blood group and RH incompatibility
  • Neonates with G6PD deficiency
  • Neonates with history of maternal phenobarbital consumption
  • Neonates with respiratory distress and signs and symptoms of sepsis

Investigators

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