Early Predictors of Necrotizing Enterocolitis in Neonates

Status Recruiting

Clinical Trial Summary

The goal of this project is to identify neonates who are predisposed to Necrotizing Enterocolitis (NEC). the investigators will determine the effectiveness of non-invasive measures as well as biochemical markers to identify neonates early in the disease process. Thus, the investigators aim to identify infants with NEC prior to the onset of symptoms to institute or test treatments in the long term to prevent the progression of the disease in these infants.

Clinical Trial Description

The study will enroll premature, low birth weight infants in the Neonatal Intensive Care Units (NICU). Potential study subjects will be identified upon delivery, or transfer to the NICU, and notification by the neonatology service. Infants born at less than 30 weeks gestational age, birth weight less than or equal to 1500 grams will be eligible for enrollment in the study. The purpose of the study designed is to compare the splanchnic tissue oxygenation index and gut inflammatory biomarkers of patients with any stage of NEC with healthy controls. Since we will not be able to determine which patients will develop NEC a priori, we will anticipate enrolling up to 450 neonates to identify 15 neonates with NEC. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03210831
Study type	Observational
Source	Nationwide Children's Hospital
Contact	Theresa Pennington
Phone	614-355-6736
Email	Theresa.Pennington@nationwidechildrens.org
Status	Recruiting
Phase
Start date	September 6, 2017
Completion date	December 2026

View Details

See also
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