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Comparison of continuous versus intermittent enteral nutrition in critically ill patients (COINN): study protocol for a randomized comparative effectiveness trial
O. Hrdy, K. Vrbica, E. Strazevska, P. Suk, L. Souckova, R. Stepanova, I. Sas, R. Gal
Language English Country Great Britain
Document type Clinical Trial Protocol, Journal Article
NLK
BioMedCentral
from 2000-04-01
BioMedCentral Open Access
from 2006
Directory of Open Access Journals
from 2006
Free Medical Journals
from 2006
PubMed Central
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Europe PubMed Central
from 2006
ProQuest Central
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Open Access Digital Library
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Open Access Digital Library
from 2006-01-01
Medline Complete (EBSCOhost)
from 2009-01-01
Nursing & Allied Health Database (ProQuest)
from 2000-04-01
Health & Medicine (ProQuest)
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ROAD: Directory of Open Access Scholarly Resources
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Springer Nature OA/Free Journals
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- MeSH
- Adult MeSH
- Enteral Nutrition * adverse effects MeSH
- Intensive Care Units MeSH
- Critical Illness * MeSH
- Humans MeSH
- Diarrhea MeSH
- Randomized Controlled Trials as Topic MeSH
- Vomiting MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial Protocol MeSH
BACKGROUND: Enteral nutrition is part of the treatment of critically ill patients. Administration of enteral nutrition may be associated with signs of intolerance, such as high gastric residual volumes, diarrhea, and vomiting. Clinical trials regarding the effects of the mode of administration of enteral nutrition on the occurrence of these complications have yielded conflicting results. This trial aims to investigate whether the mode of administration of enteral nutrition affects the time to reach nutritional targets, intolerance, and complications. METHODS: COINN is a randomized, monocentric study for critically ill adult patients receiving enteral nutrition. Patients will be randomly assigned to two groups receiving (1) continuous or (2) intermittent administration of enteral nutrition. Enhancement of enteral nutrition will depend on signs of tolerance, mainly the gastric residual volume. The primary outcome will be the time to reach the energetic target. Secondary outcomes will be the time to reach the protein target, tolerance, complications, hospital and ICU lengths of stay, and 28-day mortality. DISCUSSION: This trial aims to evaluate whether the mode of application of enteral nutrition affects the time to reach nutritional targets, signs of intolerance, and complications. TRIAL REGISTRATION: ClinicalTrials.gov NCT03573453. Registered on 29 June 2018.
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