Optimal Feeding Tube Placement

Status Completed

Clinical Trial Summary

A randomized controlled trial comparing current standard blind method to CORTRAK enteral access system (CEAS), an FDA approved electromagnetic device to place enteric tubes.

Clinical Trial Description

Patient population would include patients in pediatric intensive care unit, pediatric cardiac unit, intermediate medical care unit and pediatric floor who receives postpyloric feeding tube placements. The study team are going to monitor total time and number attempts required for each successful placement, correlation of findings on x-ray versus CEAS, cost-effectiveness of this new equipment with standard blind method and decrease in radiation exposure with CEAS. ;

Study Design

Related Conditions & MeSH terms

Enteral Feeding Intolerance

Clinical Trial Details

NCT number	NCT04241146
Study type	Interventional
Source	The University of Texas Health Science Center at San Antonio
Contact
Status	Completed
Phase	N/A
Start date	January 6, 2018
Completion date	November 21, 2019

View Details

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