Skip to content

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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190708044158N1
Enrollment
80
Registered
2020-02-01
Start date
2019-11-08
Completion date
Unknown
Last updated
2020-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neonatal jaundice. Neonatal jaundice from other and unspecified causes

Interventions

Intervention 1: Fenofibrate group: single dose of oral fenofibrate (Sobhan Co., Iran) in liquid form, containing 20 mg/ml, with a dose of 10 mg/kg was given at the time of admission. Standard photothe

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Days to 28 Days

Inclusion criteria

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

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

Design outcomes

Secondary

MeasureTime frame
Duration of need to phototherapy and hospital stay. Timepoint: From the time of admission until discharge. Method of measurement: Duration of time by hour.

Primary

MeasureTime frame
Serum bilirubin level. Timepoint: Admission time, second day, third day, discharge time. Method of measurement: Spectrophotometric method with the biochemical kit ( made in Iran ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMousa Ahmadpour-kacho

Babol University of Medical Sciences

mousa_ahmadpour@hotmail.com+98 11 3235 4951

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026