N/A N=52 Randomized Treatment

Optimal Feeding Tube Placement

Enteral Feeding Intolerance

Bottom Line

View on ClinicalTrials.gov: NCT04241146 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Feb 2020

Primary outcome: Primary: Duration of Time — 19; 2.5 Minutes

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Enteric Tube (Device); CORTRAK enteral access system (Device)
Age: Pediatric, Adult
Sex: All
Sponsor: The University of Texas Health Science Center at San Antonio
Primary completion: Oct 2018

Outcome Measures

Outcome	Result	p-value
PRIMARY Duration of Time	19; 2.5	—
SECONDARY Number of X-Rays	2; 1	—

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.

Eligibility Criteria

Inclusion Criteria: Patient admitted to pediatric floor, intermediate care unit, pediatric intensive care unit, or congenital care unit requiring post-pyloric feeding tube placement of size eight french or more and not meeting any of exclusion criteria Exclusion Criteria: Under three kilograms, Open chest wall, Open abdominal wall

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04241146). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.