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Malnutrition clinical trials

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NCT ID: NCT02987569 Completed - Malnutrition Clinical Trials

Teen and Young Adult Connections for Support From Multidisciplinary Professionals & Peers

Start date: July 2016
Phase: N/A
Study type: Interventional

12 month study testing mobile delivery of health information and connections to professionals and peers to improve health of teen/young adult HPN users.

NCT ID: NCT02987335 Completed - Diabetes Clinical Trials

Metabolic Characteristics of Lean Diabetes in Rural and Semi-urban India and in the United States

Start date: December 2010
Phase:
Study type: Observational

This purpose of this study is to define the metabolic characteristics of individuals with Lean Diabetes. We aim to determine whether differences in body composition, including any differences in lipid (fat) deposition, exist compared to individuals with either known forms of diabetes (eg, type 1 and type 2), or individuals without diabetes. Diabetes affects the ability of the body to process glucose (sugar). Therefore, we also plan to investigate the ability of the hormone insulin to regulate changes in glucose in these individuals. Developing a greater understanding of the features of this condition could have tremendous therapeutic benefit for these individuals.

NCT ID: NCT02985359 Completed - Undernutrition Clinical Trials

Impact Evaluation of the WFP-Implemented Nutrition Program in Malawi

Start date: January 2014
Phase: N/A
Study type: Observational

The goal of this evaluation is to assess the impact of a 3.5 year, World Food Program (WFP) supplemental child feeding and nutrition services program in reducing stunting and improving linear growth in children from 6 through 24 months of age in a rural district of Malawi.

NCT ID: NCT02962089 Completed - Undernutrition Clinical Trials

Microbiota and Protein-energy Wasting (MIDIWA)

MIDIWA
Start date: August 2016
Phase: N/A
Study type: Interventional

Oral supplementation with branched chain amino acids (BCAA) increases the levels of circulating BCAA, stimulates BCAA uptake in muscles, and decreases amino acid release from muscle, eventually promoting muscle anabolism. However, uptake of oral BCAA by muscle is not complete, pointing out that non-muscular tissues, as the splanchnic bed and gut microbiota, may play a role in BCAA metabolism. This protocol aims at studying the impact of protein-energy wasting (PEW) and of refeeding with branched chain amino acids (BCAA), on gut barrier including gut microbiota, in chronic hemodialysis (HD) patients. The investigators speculate that: 1. HD patients with PEW have altered composition and function of gut microbiota, increased permeability of epithelial gut barrier, increased systemic inflammation but decreased fecal immunoglobulin A (IgA), and a dysbalance of plasma appetite mediators in favor of anorexigenic mediators, compared to HD patients without PEW, non dialyzed patients with chronic kidney disease and well-nourished non obese subjects, 2. BCAA supplementation of HD patients with PEW reverses these changes, thereby improving nutritional state, physical function, quality of life and resistance to infections.

NCT ID: NCT02961205 Completed - Malnutrition Clinical Trials

Nutrition Supplementation in Cardiovascular Surgery Patients

NutriSuP-CVS
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

This randomized controlled pilot study evaluates the use of oral nutritional supplementation in nutritionally at-risk cardiovascular surgery patients. The oral nutrition supplement is given for 30 days prior to surgery, continuing throughout their surgical hospitalization and ends at hospital discharge. Half of the participants will receive the oral nutritional supplement and the other half will not.

NCT ID: NCT02938247 Completed - Malnutrition Clinical Trials

Tolerance and Compliance of a High Caloric, High Protein Oral Nutritional Supplement - Scheduled Intake

Start date: September 2016
Phase: N/A
Study type: Interventional

The aim of the study is to assess gastro-intestinal tolerance, palatability, compliance, and use of a high caloric, high protein oral nutritional supplement (ONS) in elderly people

NCT ID: NCT02938234 Completed - Malnutrition Clinical Trials

Tolerance and Compliance of a High Caloric, High Protein Oral Nutritional Supplement - Free Intake

Start date: September 2016
Phase: N/A
Study type: Interventional

The aim of the study is to assess gastro-intestinal tolerance, palatability, compliance, and use of a high caloric, high protein oral nutritional supplement (ONS) in elderly people

NCT ID: NCT02923804 Completed - Clinical trials for Non Alcoholic Fatty Liver

Evaluation of MF4637 for Correcting the Omega-3 Nutritional Deficiency in NAFLD Patients

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

This study is a prospective, randomized, placebo-controlled, double-blind trial to determine the effect of high concentrate omega-3 capsules on the omega-3 status of patients with non-alcoholic fatty liver.

NCT ID: NCT02914002 Completed - Malnutrition Clinical Trials

Psychoeducational Intervention Model to Improve Nutritional Status in Low Resource Settings

Start date: June 2016
Phase: N/A
Study type: Interventional

Comer en Familia is a psychoeducational intervention in nutrition aimed to improve nutritional status in families, particularly mothers and caregivers of children between the ages of 5 and 13 years and their children through providing healthy cooking lessons in their communities where the optimal preparation and use of local foods based on vegetables is promoted at the same time the importance of cooking at home and eating as a family is highlighted.

NCT ID: NCT02911246 Completed - Malnutrition Clinical Trials

Evaluation Report of the Urea / Urine Creatinine as a Marker of Nutritional Status Predictive of ICU Care Associated Infections

UREA
Start date: December 2014
Phase: N/A
Study type: Observational

Malnutrition is defined by an energy supply deficit, protein, macro-molecules or micro-nutrients, resulting from an imbalance between nutrient intakes and metabolic needs of the body. It concerns 40 to 60% of patients upon entry into resuscitation and influences their prognosis. Studies over the past decade have shown that nutritional deficiency increases the morbidity and mortality in intensive care. Several clinical and biological parameters were evaluated as markers of malnutrition, including the ratio of urea / urine creatinine. The report would identify patients in a state of malnutrition, to optimize their nutritional care. This setting is easy to obtain in all patients by simple urine collection unlike other clinical and biological criteria of resuscitation malnutrition assessment. This ratio of urea / urien creatinine would optimize energy intake of critically ill patients, for which nutritional management methods are widely debated.