Enteral Feeding Intolerance Clinical Trial
Official title:
A Randomized Controlled Trial for Optimal Feeding Tube Placement
Verified date | February 2020 |
Source | The University of Texas Health Science Center at San Antonio |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A randomized controlled trial comparing current standard blind method to CORTRAK enteral access system (CEAS), an FDA approved electromagnetic device to place enteric tubes.
Status | Completed |
Enrollment | 52 |
Est. completion date | November 21, 2019 |
Est. primary completion date | October 10, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A to 18 Years |
Eligibility |
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 |
Country | Name | City | State |
---|---|---|---|
United States | University Hospital | San Antonio | Texas |
Lead Sponsor | Collaborator |
---|---|
The University of Texas Health Science Center at San Antonio | Avanos Medical |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Duration of Time | Time taken for placement of enteral tube | Baseline to End of procedure up to 30 minutes | |
Secondary | Number of X-Rays | Number of X-rays required to achieve correct tube placement | Baseline to End of procedure up to 30 minutes |
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