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Use of ReliZORB for Feeding Intolerance in Critically Ill Patients

Critical Illness Clinical Trial

Official title:
Single-center, Open-label, Prospective Randomized (Double-Blind) Study on the Use of ReliZORB™ for the Treatment of Feeding Intolerance in Critically Ill Adults With Multi Organ Failure

Clinical Trial Summary

The purpose of this study is to determine if the use of ReliZORB improves nutrition tolerance and helps critically ill patients meet their nutrition goals. Subjects in the intensive care unit will be enrolled and randomized 2:1 to receive ReliZORB or placebo cartridges with enteral feedings for 5 days. Blood and stool samples will be collected to test for nutrition and inflammation.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05710315
Study type Interventional
Source Duke University
Contact
Status Withdrawn
Phase Phase 4
Start date May 1, 2023
Completion date January 30, 2024
View Details
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