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Evaluation of probiotics effects on bilirubin level

Phase 1
Conditions
neonatal hyperbilirubinemia.
P59.9 Neonatal jaundice, unspecified Physiological jaundice (intense)(prolonged) NOS
Registration Number
IRCT2017061018974N3
Lead Sponsor
Deputy Minister for Research and Technology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
70
Inclusion Criteria

term infants with age between 3-10 days and gestational age of 42-37 weeks , birth weight equals or more than 2500 g , and bilirubin 12.9-up mg / dL at the start of phototherapy, and fed only by breast milk.Exclusion criteria: infants with blood disorders family, having signs of hemolysis due to blood group incompatibility, internal bleeding indoors due to complications of traumatic birth (exp : cephalohematom), suspected neonatal infection such as chorioamnionitis, intrauterine infection, sepsis and urinary tract infection, perinatal hypoxic newborns, having thyroid dysfunction, distress or respiratory failure, malfunction regulate body temperature and metabolic, hemodynamic instability and congenital heart disease, a history of maternal use of phenobarbital during the last month of pregnancy venous hematocrit 65%

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bilirubin level. Timepoint: from 1 to 4 days. Method of measurement: serum lilirubin level.
Secondary Outcome Measures
NameTimeMethod
Defecations times. Timepoint: 1 and 4 days. Method of measurement: mother report.
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