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Enteral Feeding clinical trials

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NCT ID: NCT02006953 Terminated - Enteral Nutrition Clinical Trials

Bolus Versus Continuous Feeding Regimens Post Gastrostomy Tube Placement

Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the best way to feed children after they have a gastrostomy tube placed. The study compares bolus feeding to continuous feeding.

NCT ID: NCT01665664 Not yet recruiting - Enteral Feeding Clinical Trials

Hypocaloric vs. Full Energy Enteral Feeding in Critically Ill Patients

Start date: September 2012
Phase: N/A
Study type: Interventional

Underfeeding in the critically ill patient is a common observable fact throughout intensive care units. Patients who develop caloric deficit during their stay in the ICU have been shown in previous reports to be associated with increased complications such as increased rate of infections, and nosocomial blood stream infections. Yet, other studies have shown that patients with moderate caloric deficit may be associated with better outcome than patients who receive higher levels of caloric intake.

NCT ID: NCT01557673 Completed - Diarrhoea Clinical Trials

Effects of Bolus and Continuous Nasogastric Feeding on Small Bowel Water Content and Blood Flow

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

Following surgery some patients are unable to swallow. For those requiring nutritional support a tube is sometimes passed through the nose into the stomach to provide feeding. Traditionally this type of feeding is given slowly over the course of the day. However, it is thought that this mode of feeding might increase the amount of fluid entering the bowel contributing to symptoms of diarrhoea. An alternative strategy of feeding, given in larger volumes in a shorter space of time resembles normal feeding patterns and may reduce the amount of water entering the bowel. In this study we want to use a non invasive medical imaging technique called "magnetic resonance imaging" (or MRI) to look at the volume of bowel water following these two feeding strategies in 12 healthy volunteers. Each volunteer will have a tube inserted into the stomach via the nose and undergo the two feeding strategies at least 7 days apart. We will take repeated images using the MRI scanner to assess the bowel response and some samples of blood are required for analysis of blood sugar.

NCT ID: NCT01448135 Completed - Critical Illness Clinical Trials

Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral Feeding Formula Versus a Standard Formula In Multiple Intensive Care Unit Settings

Start date: October 2011
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to assess the efficacy, safety and tolerance profile of the enteral feeding product VITAL AF (a semi-elemental, high protein, and high omega-3 fish oil) when compared to Osmolite 1.2, a standard feeding product in critically ill and/or post surgical patients in the intensive care unit (ICU). If enough patients are recruited, inferences about impact on outcomes may also be drawn.

NCT ID: NCT00480259 Completed - Enteral Feeding Clinical Trials

Hyperproteic Nutrition:Correlation of BUN to Nitrogen Balance

Start date: June 1, 2007
Phase: N/A
Study type: Interventional

This study is designed to determine if the following are true. When protein requirements exceed metabolic requirements, blood urea nitrogen(BUN) levels will rise. Elevated BUN levels in the absence of renal failure, hepatic failure, or GI bleeding, will be correlated with improved nitrogen balance and inversely correlated with infection rates, days of mechanical ventilation, ICU days, and total hospital days.

NCT ID: NCT00345566 Not yet recruiting - Cerebral Palsy Clinical Trials

Effect of Protein Composition on Gastric Emptying

Start date: August 2006
Phase: N/A
Study type: Interventional

The protein composition of nutrition may affect the rate of gastric emptying and gastric fysiology. This is espesially important in children with neurologic impariment, who commonly rely on tube feedings, have feeding problems, nausea, vomiting, gastroesophageal reflux and delayed gastric emptying. We aim to find out whether 4 different protein sources affect the rate of gastric emptying and electrofysiology in this group of children.

NCT ID: NCT00213668 Completed - Enteral Feeding Clinical Trials

Effect of Glutamine on Gastric Emptying and Length of Parenteral Nutrition in Premature Neonates

Start date: April 2002
Phase: Phase 4
Study type: Interventional

This study investigates the effects of enterally supplied glutamine on gastric emptying, intestinal transit, age of total enteral nutrition and age at the end of hospitalisation. Forty neonates, aged at least 2 days and free of acute illness participate in a prospective, randomised, double-blind study. All are fed with parenteral and enteral nutrition enriched with glutamine (0.7 g/kg/per day, group 1) or isonitrogenous control (group 2). Gastric emptying is analysed by sequential measure of intragastric residue by diluted polyethylene glycol (PEG) 4000. Intestinal transit is analysed by Rouge Carmin test.