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Clinical Trials/NCT02116699
NCT02116699
Completed
Not Applicable

Oropharyngeal Administration of Mother's Colostrum: Health Outcomes of Premature Infants

NorthShore University HealthSystem5 sites in 1 country260 target enrollmentNovember 20, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infection
Sponsor
NorthShore University HealthSystem
Enrollment
260
Locations
5
Primary Endpoint
Incidence of necrotizing enterocolitis
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Extremely premature (BW<1250g) infants are at high risk for morbidity and mortality. Own mother's colostrum (OMC) and milk (OMM) protect against neonatal morbidity and are rich in immune factors which may provide immunostimulatory effects when administered oropharyngeally to extremely premature infants during the first weeks of life. The investigators hypothesize that infants who receive oropharyngeal mother's colostrum and milk will have significantly lower rates of infection and improved health outcomes, compared to infants who receive a placebo.

Detailed Description

Extremely premature (BW\<1250g) infants are at high risk for morbidity and mortality. Own mother's colostrum (OMC) and milk (OMM) protect against neonatal morbidity and are rich in immune factors which may provide immunostimulatory effects when administered oropharyngeally to extremely premature infants during the first weeks of life. This 5-year placebo-controlled, double-blind randomized controlled trial will evaluate the safety, efficacy and health outcomes of oropharyngeal administration of OMC/OMM in a sample of 622 (total patients enrolled) extremely premature infants with the following aims: Aim 1. To determine if oropharyngeal administration of OMC/OMM to extremely premature infants will reduce the risk of late-onset sepsis or death as the primary outcome, and necrotizing enterocolitis and ventilator-associated pneumonia as pre-planned secondary outcomes. Aim 2: To determine if extremely premature infants who receive OMC/OMM via the oropharyngeal route have a shorter time to reach full enteral feeds and a shorter length of hospital stay. Aim 3: To determine if oropharyngeal administration of OMC/OMM will have immunostimulatory effects for extremely premature infants, as measured by (A) enhancement of gastrointestinal (fecal) microbiota, (B) improvement in antioxidant defense maturation or reduction of pro-oxidant status, and (C) maturation of immunostimulatory effects as measured by changes in urinary lactoferrin. Results will confirm whether extremely premature infants demonstrate a host-immune response to this intervention and whether there is a beneficial effect on common morbidities in these high risk patients.

Registry
clinicaltrials.gov
Start Date
November 20, 2013
End Date
January 4, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Birthweight \<1250g Mother plans to pump and provide breastmilk for at least 2 months Absence of severe congenital anomalies Admission to the neonatal intensive care unit within 24 hours after birth Ability to begin protocol within 96 hours of life

Exclusion Criteria

  • Gastrointestinal anomaly pH \< 7.0 on initial blood gas in NICU Maternal +HIV status Maternal drug or substance use that precludes infant from receiving mother's milk Tracheoesophageal fistula

Outcomes

Primary Outcomes

Incidence of necrotizing enterocolitis

Time Frame: at 40 weeks CGA

defined according to modified Bell's criteria stage \>2 with clinical signs and radiological evidence of pneumatosis intestinalis or portal venous gas

Incidence of ventilator-associated pneumonia

Time Frame: at 40 weeks CGA

Incidence of of late-onset sepsis

Time Frame: at 40 wks CGA

positive blood cultures (not deemed contaminated) collected after 72 hours of age, and 2 clinical symptoms

Secondary Outcomes

  • Time to reach full enteral feeds(at 40 wks CGA)
  • Changes in stool microbiome(3 days, 2 weeks, 32 weeks CGA)
  • Length of hospital stay(at 40 wks CGA)
  • Concentrations of lactoferrin in urine(1 day, 3 days, 32 weeks CGA)
  • Changes in urinary biomarkers of oxidative stress(3 days,)

Study Sites (5)

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