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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05121753
Other study ID # NEC_1121
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 15, 2022
Est. completion date January 15, 2024

Study information

Verified date February 2022
Source Neuroganics LLC
Contact Donald Cooper, Ph.D.
Phone 720.580.8343
Email NECstudy@protonmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date January 15, 2024
Est. primary completion date January 15, 2024
Accepts healthy volunteers No
Gender All
Age group N/A to 2 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Survey investigating Infant formula feeding in newborns
A database will be created that allows individuals to register and enter information about the premature infant's feeding history and symptoms/ medical history.

Locations

Country Name City State
United States 10190 Bannock St #102 Northglenn Colorado

Sponsors (2)

Lead Sponsor Collaborator
Neuroganics LLC Ramos Law Injury Firm

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Infant formulas and increased risk for NEC survey 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. 2 years
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