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A prospective study on The additive effect of ursodeoxycholic acid on indirect hyperbilirubinemia in neonate under phototherapy

A prospective study on The additive effect of ursodeoxycholic acid on indirect hyperbilirubinemia in neonate under phototherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013020512370N1
Enrollment
80
Registered
2013-05-12
Start date
2012-12-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Indirect hyperbilirubinemia in neonate. Physiological jaundice (intense)(prolonged) NOS

Interventions

Intervention 1: First group was given ursodeoxycholic acid 10-15 mg/kg divided q12h before starting phototherapy till exclusion from study. In the first day, laboratory tests included estimation of to
Treatment - Drugs
First group was given ursodeoxycholic acid 10-15 mg/kg divided q12h before starting phototherapy till exclusion from study. In the first day, laboratory tests included estimation of total bilirubin (d
Second group that is control group received no medications and only underwent phototherapy.

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 28 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: birth-weight 2500-4000 gr; gestational age between 38-41 weeks; breastfeeding neonate; total bilirubin 14-20 mg/dl and neonates age older than three days. Exclusion criteria: infants with incompatible ABO, Rh; G6PD deficiency; direct hyper billirubinemia; septicemia or diseases that are implicated in causing jaundice; premature infants; infants of diabetic mothers.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of need phototherapy. Timepoint: Since start study till finish study. Method of measurement: Timer.

Secondary

MeasureTime frame
Serum total bilirubin. Timepoint: Since start study &12, 24, 36, 48 hour. Method of measurement: Blood sample.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGhashghaei Saadi Elham MD

Shiraz University of Medical Sciences

elhamghashghaei @yahoo.com; ghashghaei@sums.ac.ir+98 71 1612 5477

Outcome results

None listed

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