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The effect of Purgative meinna and clofibrate on neonatal hyperbilirobinemia

The effect of Purgative meinna and clofibrate on neonatal hyperbilirobinemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016110412897N2
Enrollment
60
Registered
2016-11-19
Start date
2016-12-21
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

jaundice. neonatal jaundice

Interventions

Intervention 1: The case group(B) will receive phototherapy and purgative meinna .The phototherapy apparatus will be Tosan model with 8 lamps made in Iran ( Life span of each lamp 2500 hours, wave l
Treatment - Drugs
The case group(B) will receive phototherapy and purgative meinna .The phototherapy apparatus will be Tosan model with 8 lamps made in Iran ( Life span of each lamp 2500 hours, wave lengh of 42-470nm
The control group(A) will receive only phototherapy. The phototherapy apparatus will be Tosan model with 8 lamps made in Iran ( Life span of each lamp 2500 hours, wave lengh of 42-470nm ,made in Germ
The case group(C) will receive phototherapy and clofibrate .The phototherapy apparatus will be Tosan model with 8 lamps made in Iran ( Life span of each lamp 2500 hours, wave lengh of 42-470nm ,made

Sponsors

Vice Chancellor for research of Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Days to 10 Days

Inclusion criteria

Inclusion criteria: Inclusion criteria: term( gestational age between 37-42 pregnancy ) ; weight between 2500-4000gr ;age more than 2 days till 10days ; existence of nonhemolytic non-conjugated hyperbilirubinemia ;breastfeeding ;disposal of the first meconium ;bilirubin more than 12 mg/dl ; candidate for phototherapy.Exclusion criteria:neonate with hemolytic non-conjugated hyperbilirubinemia;neonate with risk factor and associated diseases;non breasfeeding infants;neonate whose mothers are suffering from diseases ; neonate with conjugated hyperbilirubinemia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bilirubin. Timepoint: Before and after intervention. Method of measurement: serum bilirubin measurement.

Secondary

MeasureTime frame
Complications. Timepoint: After intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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