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The survey of the effect of Billy Cuttermana on decreasing jaundice in neonates

A comparative study of the effect of Billynaster and Billy Cuttermana on decreasing jaundice in neonates

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015120425203N2
Enrollment
350
Registered
2016-02-18
Start date
2016-02-20
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

Neonatal Jaundice. Neonatal Jaundice, Unspecified

Interventions

Intervention 1: Control group only treated with photo therapy. Intervention 2: Intervention group one, infant received Bilikatermana 5 drops per kg of body weight three times a day in addition to the
Early detection
Treatment - Drugs
Control group only treated with photo therapy
Intervention group one, infant received Bilikatermana 5 drops per kg of body weight three times a day in addition to the phototherapy
Group two, infant received Bilineaster 5 drops per kg of body weight three times a day in addition to the phototherapy
Group three, infant and her/his mother received Bilicatermana 2 drops per kg of body weight three times a day in addition to the phototherapy (infant)
Group four, infant and her/his mother received Bilineaster 2 drops per kg of body weight three times a day in addition to the phototherapy (infant)
Group five, infants mother received Bilikatermana 5 drops per kg of body weight three times a day in addition to the phototherapy (infant)
Group six, infants mother received Bilineaster 5 drops per kg of body weight three times a day in addition to the phototherapy (infant)

Sponsors

Dezful University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Days to 14 Days

Inclusion criteria

Inclusion criteria: Inclusion criteria: Healthy term breast-fed infants weighing 2.5 to 4 Kg after 36 hours until 14 days developed jaundice and photo therapy indicated. Exclusion criteria: per-and post term infants; formula feeding; the presence of any malformations and associated diseases such as sepsis; weighing less than 2.5 and more than 4 kg; neonates developed jaundice after 14 days who need Intensive photo therapy or exchange; ABO or RH incompatibility; presence direct hyper bilirubinemia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bilirubin. Timepoint: On arrival at the hospital, 12, 24, 48, 72 hours after it. Method of measurement: Bailey Test milligrams per deciliter.

Secondary

MeasureTime frame
Bilirubin. Timepoint: 12, 24, 48, 72 hours after it. Method of measurement: Bailey Test milligrams per deciliter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamidreza Aghababaeian

Dezful University Of Medical Sciences, Dezful, Iran

AGHABABAEIAN.H@DUMS.AC.IR+98 61 4242 9733

Outcome results

None listed

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