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Outcome of Saccharomyces boulardii prophlaxis on necrotizing enterocolitis

Phase 3
Conditions
ecrotizing eneterocolitis, neonatal sepsis.
Necrotizing enterocolitis of fetus and newborn, bacterial sepsis of newborn
P77, P36
Registration Number
IRCT2012071410279N1
Lead Sponsor
Health Ministry Drug and Pharmacy General Management
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
208
Inclusion Criteria

Very low birth weight infants (gestational age: =32 weeks; birth weight: =1500 g) who survived to feed enterally (minimum age: first postnatal day, maximum age: 1 week).
Exclusion criteria: Infants who had severe asphyxia (stage III), major congenital anomalies, those who had been fasted for more than 3 weeks, died within the first postnatal 14 days and infants who used antifungal therapy were excluded.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sepsis. Timepoint: Starts at the same time with the intervention. Method of measurement: Patients' medical records.;Necrotizing enterocolitis. Timepoint: Starts at the same time with the intervention. Method of measurement: Patients' medical records.
Secondary Outcome Measures
NameTimeMethod
ength of hospitalization. Timepoint: Starts at the same time with the intervention. Method of measurement: Patients' medical records.;Time to reach full enteral feeding. Timepoint: Starts at the same time with the intervention. Method of measurement: Patients medical records.;Mortality until hospital discharge. Timepoint: Starts at the same time with the intervention. Method of measurement: Patients' medical records.;Weight gain per week. Timepoint: Starts on the 7th day of intervention. Method of measurement: Patients' medical records.;Neurocognitive development. Timepoint: 18 months corrected age. Method of measurement: Bayley test.
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