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Effect of hydrolyzed formula and standard formula in the first two weeks of life in preterm infants

Phase 3
Conditions
ecrotizing enterocolitis.
Necrotizing enterocolitis in newborn, unspecified
P77.9
Registration Number
IRCT20160120026115N7
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
104
Inclusion Criteria

Infants less than 34 weeks gestationally deprived of breast milk
Infants without underlying congenital disorders

Exclusion Criteria

Infants were excluded from the study with parental dissatisfaction.
Infants from addicted parents were excluded from the study.
Infants with asphyxia were excluded from the study.
Infants with a fifth minute Apgar score of less than seven were excluded from the study.
Infants with IUG-R were excluded from the study.
Infants with congenital anomalies were excluded from the study.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement in nutritional tolerance. Timepoint: From the start of feeding the baby to the time of discharge from the hospital. Method of measurement: Clinical examination corresponding to the disease.;Reducing the incidence of necrotizing enterocolitis in premature infants. Timepoint: From the start of feeding the baby to the time of discharge from the hospital. Method of measurement: Clinical and laboratory examination corresponding to the disease.
Secondary Outcome Measures
NameTimeMethod
Duration of hospital stay. Timepoint: From the start of feeding the baby to the time of discharge from the hospital. Method of measurement: Number of days of hospitalization based on the contents of the file.;Sepsis. Timepoint: From the start of feeding the baby to the time of discharge from the hospital. Method of measurement: Positive blood culture.
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