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Role of Fenofibrate in Neonatal Jaundice

A

Ain Shams University

Status and phase

Completed
Phase 4

Conditions

Neonatal Jaundice

Treatments

Drug: Fenofibrate
Other: placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT06451900
prophylactic fenofibrate

Details and patient eligibility

About

Fenofibrate appears to be an effective and safe drug for the treatment of neonatal hyperbilirubinemia. It has been proven that it decreases the duration of phototherapy and thus shortens the length of hospital stay.

This study was performed to study the prophylactic role of fenofibrate in prevention of neonatal jaundice.

Full description

Neonatal jaundice is a common disease in neonates. Based on current statistics, 60% of term neonates and 80% of preterm neonates suffer from jaundice during the first week of birth The normal bilirubin level of the umbilical cord is 1-3 mg/dL, which increases to 5-6 mg/dL on the second to fourth days after birth and decreases to less than 2 mg/dL on the 5th to 7th days after birth .

Destruction of red blood cell and its hemoglobin component produces bilirubin which is then conjugated to a soluble form and excreted. In neonates, this becomes more significant because of high red cell mass and relative immaturity for bilirubin conjugation.

Free bilirubin deposits in the skin and mucous membranes and produces jaundice. It may also deposit in the brain where it has been implicated in causing transient dysfunction and, occasionally, permanent neuronal damage.

Every year, a huge hospital cost is imposed on parents for the treatment of neonatal jaundice. Moreover, it leads to the mother-child separation and subsequent mental health problems. Proven treatments for jaundice include phototherapy and blood exchange transfusion in which each one has its own complications . medication has also been used to prevent and treat neonatal jaundice Including IVIG, protoporphyrin, phenobarbital and fenofibrate.

Fibrates have been used for several years as a hypolipidemic drug in adults.They exert their hypolipidemic activity through peroxisome proliferator- activated receptor activation The value of this mechanism in the reduction of bile acid synthesis had been demonstrated by experimental study of cindrouk and colleagues . Fibrates also increase bilirubin conjugation and excretion via induction of glucuronyl transferase activity. Its potency to induce bilirubin conjugation is very high. Fibrates are aclass of phenoxy iso butyric acid derivatives including clofibrate and fenofibrate. Fenofibrate is one of the fibrates it has inducing effect on glucuronyl transferase activity, it increases bilirubin conjugation and excretion making it possible to be used in the treatment of neonatal jaundice via influencing bilirubin metabolism. Fenofibrate is very similar to clofibrate in its action. However, it is simply more accessible and has more safety profile, therefore, it is much safer to be given to children than clofibrate. Fenofibrate has been used in treatment of neonatal jaundice the researchers aim to explore its efficiency as a prophylactic agent in neonates with neonatal jaundice not reaching the level of phototherapy.

Enrollment

75 patients

Sex

All

Ages

1 to 28 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • full-term (37 to 41 weeks),
  • Appropriate for gestational age weight between 2500 to 3500 gm infants
  • neonatal hyperbilirubinemia not reaching the level of phototherapy.

Exclusion criteria

  • Newborns with congenital malformations.
  • Conjugated hyperbilirubinemia.
  • Newborns who need exchange transfusion and phototherapy.
  • Newborns presenting with ABO or Rh incompatibility.
  • G6PD deficiency.
  • Newborns with skin abrasions or infections.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

75 participants in 3 patient groups, including a placebo group

fenofibrate single dose
Experimental group
Description:
full term neonates will receive a single oral dose of 10 mg/kg of non- micronized fenofibrate
Treatment:
Drug: Fenofibrate
fenofibrate double dose
Experimental group
Description:
full term neonates will receive two oral doses of 10 mg/kg of non - micronized fenofibrate.
Treatment:
Drug: Fenofibrate
placebo
Placebo Comparator group
Description:
full term neonates will receive equivalent amount of distilled water.
Treatment:
Other: placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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