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Clinical Trials/NCT05121753
NCT05121753UnknownNot Applicable

Infant Formula Feeding and the Etiology of Necrotizing Enterocolitis in Newborns Survey

Neuroganics LLC1 site in 1 country1,000 target enrollmentStarted: February 15, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
1,000
Locations
1
Primary Endpoint
Infant formulas and increased risk for NEC survey

Study Overview

Brief Summary

Necrotizing enterocolitis (NEC) is the most common life-threatening gastrointestinal emergency of prematurity, associated with a significant morbidity and mortality. Early diagnosis and early treatment interventions may reduce the risk of mortality and morbidity.

The Primary goal of this observational study is to gather survey data to establish a national database of NEC in newborns in order to better understand the risk factors underlying NEC. Survey data will be used along with a medical history to identify the mechanism(s) underlying the increased prevalence of NEC in non-breast fed, formula fed premature infants.

Detailed Description

NEC affects between 2 to 7% of premature infants. It is is an acquired disease, caused, in part by inflammation of the intestinal lining. NEC is the most common life-threatening gastrointestinal emergency of prematurity and it is associated with significant morbidity and mortality.

Studies have linked the consumption of non-breast milk, commercial infant formula (made from cow's milk) or formula-derived nutrition with increased risk of NEC compared to consumption of human breast milk.

The mechanism of the NEC lesions appears to involve factors including allergic reaction to the infant formulas containing cow's milk, immaturity of the intestinal barrier and the immune system, microvascular imbalance, disturbed gut flora and systemic inflammation that is hypothesized to be exacerbated by infant formula consumption.

The primary goal of this National observational study is to gather survey data in order to establish a database of NEC in newborns to gain a better understanding of the risk factors underlying NEC. Survey data will be used along with a medical history to identify the mechanism(s) underlying the increased prevalence of NEC in non-breast fed, formula fed premature infants.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Other

Eligibility Criteria

Ages
1 Day to 2 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Infants born after 2018
  • Newborns that have been diagnosed with NEC and have consumed infant formula.
  • Infants whose death resulted from NEC or complications thereof

Exclusion Criteria

  • Infants who were born prior to 2019
  • Newborns who have been fed exclusively on breast milk.
  • Subjects lacking medical records or who cannot provide a medical history.

Outcomes

Primary Outcomes

Infant formulas and increased risk for NEC survey

Time Frame: 2 years

A survey is given to allow parents/ guardians or health care workers to describe the events leading up to the development of NEC in their newborn.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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