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Enteral Feeding Intolerance clinical trials

View clinical trials related to Enteral Feeding Intolerance.

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NCT ID: NCT06076460 Recruiting - Clinical trials for Enteral Feeding Intolerance

Early Total Enteral Feeding Versus Convention Enteral Feeding in Preterm Infants 27-32 Weeks of Gestation

ETEFVsCEF
Start date: March 11, 2022
Phase: N/A
Study type: Interventional

The objective of the study is to compare the time of attainment of full enteral feeds in preterm neonates between 27-32 weeks of gestation started on early total enteral feeding (ETEF) with those started on conventional enteral feeding (CEF).

NCT ID: NCT05828758 Recruiting - Clinical trials for Enteral Feeding Intolerance

Amoxicillin for Enteral Nutrition Intolerance in Pediatric Intensive Care Unit

AmoxENI
Start date: April 24, 2023
Phase: Phase 2/Phase 3
Study type: Interventional

The goal of this randomized controlled study is to investigate the efficacy of enteral amoxicillin for the treatment of children with feeding intolerance in pediatric intensive care unit. Children with feeding intolerance will be randomized into study and comparison groups. The study group will receive amoxicillin 10 mg/kg by nasogastric tube 3 times daily 10 minutes before bolus gastric feeding for 7 days. The comparison group will receive equal volume of distilled water as a placebo. The primary outcome will be the improvement of feeding intolerance on day 7 study timepoint.

NCT ID: NCT05271565 Recruiting - Clinical trials for Enteral Feeding Intolerance

The Influence of Polymeric Versus Oligomeric Enteral Feeding on Tolerance and Nutritional Status in Paediatric Intensive Care Pilot

Polygomerpilot
Start date: April 21, 2022
Phase: N/A
Study type: Interventional

Malnutrition is associated with negative impact on morbidity and mortality of critically ill patients. Therefore, in patients unable of peroral intake, the nutritional support is indicated. The preferred form of nutritional support is enteral, the more natural form, compared to parenteral. The enteral nutrition is cheaper and is associated with better outcomes and lower incidence of associated complications. The intolerance of enteral feeding is common in critically ill patients, and is associated with insufficient energy and protein intake, that could be linked with the complications such aspiration pneumonia. The optimization of enteral feeding tolerance is therefore one of the research priorities. Implementation of feeding protocols is associated with better tolerance. The enteral feeding could be administered as a oligomeric or polymeric formula. The are preliminary data from adult population pointing at better tolerance of oligomeric feeding formula.

NCT ID: NCT05265143 Recruiting - Clinical trials for Enteral Feeding Intolerance

Comparision of Two Different Feeding Method in Preterms

Start date: January 1, 2015
Phase: N/A
Study type: Interventional

achievement of optimal postnatal growth by adequate enteral nutrition in critically ill preterm infants is a challenge of NICU. signs like abdominal distension, reflux, vomiting, nec is a factors of discontinuing fedding in preterm. this factors plays a role in decisions about which method of gavage feeding is adopted. we compare two different feeding method to achive less fedding tolerence.

NCT ID: NCT04900597 Recruiting - Clinical trials for Enteral Feeding Intolerance

Effect of Blenderized Enteral Tube Feeds on Pediatric Upper Gastrointestinal Tract Physiology

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

Blenderized diets consist of a wide range of table foods such as fruits, vegetables, meat and legumes, pureed in a blender and administered via gastrostomy tube. In a recent study, the investigators reported that children receiving blenderized feeds via gastrostomy had fewer total admissions and respiratory admissions, total emergency room visits, and improved gastrointestinal symptom scores compared to those fed formula. The goal of this project is to understand how these diets affect gastroesophageal reflux burden.

NCT ID: NCT04551846 Recruiting - Clinical trials for Enteral Feeding Intolerance

The Influence of Polymeric Versus Oligomeric Enteral Feeding on Tolerance and Nutritional Status in Paediatric Intensive Care

Polygomer
Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Malnutrition is associated with negative impact on morbidity and mortality of critically ill patients. Therefore, in patients unable of peroral intake, the nutritional support is indicated. The preferred form of nutritional support is enteral, the more natural form, compared to parenteral. The enteral nutrition is cheaper and is associated with better outcomes and lower incidence of associated complications. The intolerance of enteral feeding is common in critically ill patients, and is associated with insufficient energy and protein intake, that could be linked with the complications such aspiration pneumonia. The optimization of enteral feeding tolerance is therefore one of the research priorities. Implementation of feeding protocols is associated with better tolerance. The enteral feeding could be administered as a oligomeric or polymeric formula. The are preliminary data from adult population pointing at better tolerance of oligomeric feeding formula.

NCT ID: NCT04013893 Recruiting - Critical Illness Clinical Trials

Evaluation of Enteral Nutrition in Critically Ill Children

Start date: June 1, 2019
Phase:
Study type: Observational

The aim of this study was to evaluate the effect of calorie and enteral feeding timing on survival in critically ill children receiving inotropic, vasopressor and inodilatory supplements.

NCT ID: NCT03795870 Recruiting - Clinical trials for Enteral Feeding Intolerance

Enteral Nutrition Tolerance and the Gut Microbiome Study

Start date: July 7, 2018
Phase: N/A
Study type: Interventional

The current study will enroll patients who are going to require enteral nutrition support for at least 4 weeks and randomize them to standard polymeric formulas or blenderized tube feeding. They will be asked to fill out a questionnaire about their tolerance of enteral feeds. They will also be asked to provide stool samples before enrollment and after 4-6 weeks. The study is trying to assess whether the use of whole food in blenderized tube feeding will be better tolerated and also lead to greater diversity of microbiome.

NCT ID: NCT03422900 Recruiting - Stroke Clinical Trials

Hyperglycemia in Patients With Stroke and Indication of Enteral Nutrition

GlyENStroke
Start date: December 12, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of a specific nutritional formula for diabetics on the development of hyperglycemia in patients with recent non-diabetic stroke who require admission and enteral nutritional support by nasogastric tube. As well as the effect on metabolic control, development of comorbidities, hospital stay, readmissions, mortality and tolerance of the formula under study.