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Parenteral Nutrition clinical trials

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NCT ID: NCT02463812 Withdrawn - Clinical trials for Parenteral Nutrition

Lipid Infusion Following Major Surgery

Start date: May 2015
Phase: N/A
Study type: Interventional

Surgery puts a lot of stress on the body, and during recovery from surgery, the body uses a lot of energy to help with healing and getting stronger. Often, sugars are given before surgery to help give the body an energy boost. Lipid solutions can also be used as an energy source and are commonly used as supplements in patients needing long-term nutrition from an intravenous route (e.g., total parenteral nutrition) when they can not eat by mouth for a medical reason. Intralipid, a solution of lipid molecules from soybeans and eggs, is commonly used for patients who need nutrition and energy supplements. The investigators wish to test whether giving Intralipid immediately after surgery can improve recovery from major surgery.

NCT ID: NCT01839617 Active, not recruiting - Cancer Clinical Trials

Study Comparing Early and Late Nutrition in Cancer Patients Undergoing Abdominal Surgery

PaNCS
Start date: May 7, 2013
Phase: N/A
Study type: Interventional

The aim of this study is to find which is the best nutritional strategy in cancer patients undergoing abdominal surgery regarding postoperative complications.

NCT ID: NCT01814956 Terminated - Clinical trials for Parenteral Nutrition

Different Lipid Emulsions in Acute Lung Injury Patients

Start date: March 2013
Phase: Phase 4
Study type: Interventional

Aim is to investigate the influence of an early supply of parenteral nutrition including a fish oil containing lipid emulsion on the course of acute lung injury in the intensive care unit. In comparison, a standard parenteral nutrition with a soybean oil based emulsion will be used. Data obtained in this trial may provide evidence for a beneficial effect of fish oil derived omega-3 fatty acids in parenteral nutrition regarding their influence on acute lung injury.

NCT ID: NCT01176695 Completed - Clinical trials for Parenteral Nutrition

Efficacy and Safety of a Fish Oil Containing Lipid Emulsion

Start date: April 2010
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare a fish oil containing lipid emulsion against a medium-chain/long-chain triglyceride (MCT/LCT) lipid emulsion in terms of their efficacy and safety during postoperative parenteral nutrition.

NCT ID: NCT00865150 Completed - Prematurity Clinical Trials

Amino Acid and Acylcarnitine Profiles in Premature Neonates

Start date: April 2009
Phase: N/A
Study type: Observational

Primary Hypotheses of the study include: - Metabolic profiles are influenced by gestational age, chronological age, type and degree of nutritional support and illness - Metabolic profiles differ between neonates who receive commercial formula and neonates who receive primarily human breast milk - Neonates who develop parenteral associated cholestasis have metabolic markers that identify at risk patients (high serum urea nitrogen, citrulline, histidine, methionine, and succinyl carnitine and low thyroxine, serine and glutamate) - Neonates that have hypothyroidism have abnormal metabolic profiles (low tyrosine levels)

NCT ID: NCT00798681 Completed - Clinical trials for Parenteral Nutrition

Evaluating the Influence of Ready-to-use (RTU) Parenteral Nutrition in the Clinical Outcome of Patients Study

EPICOS
Start date: July 2008
Phase: Phase 4
Study type: Interventional

This is an international prospective randomized multicenter open-label controlled study. The primary center will be Fernandes Távora Hospital (Fortaleza, Ceará). The aim of this study is to investigate the effects of closed parenteral nutrition systems when compared to open parenteral nutrition systems in terms of several clinical outcomes.

NCT ID: NCT00672854 Completed - Clinical trials for Parenteral Nutrition

Study Comparing a Soybean Oil-Based With an Olive Oil-Based Lipid Emulsion in ICU Patients Requiring TPN

TPN2
Start date: November 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Many hospitalized patients who are malnourished or not eating receive intravenous feeding or total parenteral nutrition (TPN). Despite improving nutrition, TPN may increase the risk of infections and hospital complications. We do not know why TPN increases hospital complications, but it may be caused by the high sugar or fat content in TPN solutions.

NCT ID: NCT00512629 Completed - Cholestasis Clinical Trials

Cholestasis Prevention: Efficacy of IV Fish Oil

Start date: July 2007
Phase: Phase 1
Study type: Interventional

Parenteral nutrition (PN) solutions are life saving in patients with surgical gastrointestinal diseases. However, the use of PN in pediatric populations, especially premature infants, is frequently associated with liver injury that may ultimately result in hepatic failure. In studies conducted in a murine model, we observed that intravenous fat emulsions (IFE) comprised of omega-3 fatty acids were able to prevent the development of cholestasis, a common precursor of PN-associated liver disease, as well as reverse preexisting PNALD through a combination of factors, including improved triglyceride clearance coupled with anti-inflammatory properties. In a case series treating patients with hepatic cholestasis, serum bilirubin levels decreased markedly after the parenteral administration of an omega-3 fatty acid based fat emulsion (Omegaven®). Patients tolerated this therapy and no adverse reactions attributed to its use were observed. Based on results of these previous studies, we propose to conduct a randomized trial aiming to gain preliminary evidence of efficacy of an omega-3 fatty acid based IFE in preventing PNALD in children with intestinal failure

NCT ID: NCT00451646 Completed - Clinical trials for Parenteral Nutrition

Study Comparing the Safety and Tolerance of SMOFlipid 20% in Long-term Treatment With Parenteral Nutrition

Start date: October 2007
Phase: Phase 3
Study type: Interventional

The aim of this study is to evaluate the safety and tolerance of SMOFlipid 20% in comparison to a standard lipid emulsion Intralipid 20% in patients requiring long-term parenteral nutrition. The safety and tolerance will be evaluated by biochemistry, hematology and coagulation variables, vital signs and adverse events. Further objectives to evaluate are the influence of SMOFlipid 20% on inflammation processes, the efficacy of anti-oxidative properties of vitamin E supplemented to SMOFlipid 20%, and the fatty acid pattern in red blood cells and serum.

NCT ID: NCT00392730 Completed - Clinical trials for Necrotizing Enterocolitis

Neurodevelopment and Neuroimaging in Parenterally-fed Infants and Young Children

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

Manganese (Mn) is an essential metal required for normal growth and development. However, exposure to high Mn levels can be toxic to the brain. The objectives of this project are to identify neonatal and young pediatric populations that are at increased risk of excessive brain Mn deposition and altered cognitive and motor development based on their dietary parenteral Mn exposure, and to make sound and evidence-based recommendations for appropriate Mn supplementation and monitoring of infants and young children receiving parenteral nutrition (PN). Our studies are designed to test the hypotheses that, compared with unexposed age-matched controls, infants and young children receiving prolonged Mn-supplemented PN will have increased deposition of Mn in their brains and lower scores on neurodevelopmental, cognitive and psychophysiological assessments.