Investigating the effect of the type of containers used in the human milk pasteurization process on preterm neonate

Not Applicable

Recruiting

Conditions: preterm neonates feeding with donor human milk.

Registration Number: IRCT20200714048101N1

Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 124

Inclusion Criteria

neonates 26-32 weeks of pregnancy
Does not have life-threatening congenital anomalies (digestive, cardiac, neurological...).
Do not have chromosomal disorders.
Do not have asphyxia.
Neonates who are fed at least 70% by donor human milk during 24 hours.
Breast milk that has not been pasteurized for more than 72 hours since leaving the refrigerator at a temperature of 4 degrees Celsius.
Donor milk that has not been stored for more than 1 month in the freezer at -20 degrees Celsius.
donor milk that has been used up to 48 hours after leaving the frozen state.
Neonates who have received donor milk up to 4 weeks after birth.
Do not have a positive blood culture at the beginning of hospitalization.

Exclusion Criteria

Transferring the neonate to different hospitals from the research environment
Death of a neonate
Parents' refusal to participate in the study
Hospitalization period less than 4 weeks

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Estrogen. Timepoint: four weeks after feeding. Method of measurement: laboratory results.

Secondary Outcome Measures

Name	Time	Method
Estrogen, growth and thyroid hormones, immunoglobulin A, anthropometric index. Timepoint: four week after feeding. Method of measurement: laboratory results.