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Undernutrition clinical trials

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NCT ID: NCT03484572 Not yet recruiting - Undernutrition Clinical Trials

Prevalence of Undernutrition in Assiut University Children Hospital

Start date: August 1, 2018
Phase:
Study type: Observational

To describe the prevalence of undernutrition in infants and children admitted to Assiut university children hospital and to describe risk group and decrease length of stay in hospital.

NCT ID: NCT03450174 Active, not recruiting - Anemia Clinical Trials

Effectiveness of Multiple Micro-nutrient Fortified Fudge on Nutritional Status of 3-5 Years of Age Children

Start date: October 2, 2017
Phase: N/A
Study type: Interventional

Multiple micro-nutrient deficiencies in Pakistan is wide spread, there is dire need to address these by using smart solutions, among them multiple fortified product (fudge) is an alternate possible way to address this issue. Fortified products have the potential to reduce micronutrient deficiencies in children, therefore in current study children from 3-5 years will receive fortified product along with enhance nutrition promotional information to bring change in their dietary practices and nutritional indices.

NCT ID: NCT03397485 Completed - Undernutrition Clinical Trials

Fortified Milk, Growth and Micronutrient Status in Mexican Toddlers (MilkGrowth)

Start date: January 1, 2011
Phase: N/A
Study type: Interventional

The objective of the present study was to assess the effect of a growing-up milk on growth and micronutrient status in children 12 to 30 months of age. The study was conducted in Cuernavaca, the state capital of Morelos, Mexico. The investigators included children who attended day-care centers. These day- care centers are part of a national government program which main objective is to support working mothers and those who intend to work and do not have access to a health service and are at risk of poverty. The study described herein is a randomized, parallel, double-blind, controlled trial by administration of growing up milk (GM) and fortified milk (FM). Results showed a significant improvement in linear growth in both supplemented groups, with no statistical difference between treatments. By using an artificial, population-based comparison group, the investigators conclude that this improvement was attributable to the supplements.

NCT ID: NCT03378141 Completed - Anemia Clinical Trials

Maternal Nutrition Interventions in Uttar Pradesh, India

Start date: November 15, 2017
Phase: N/A
Study type: Interventional

Maternal nutrition has been a long-standing concern of health authorities globally and in India. Despite the availability of proven, affordable interventions, and progressive policies and program platforms such as Maternal, Newborn and Child Health (MNCH) services, a streamlined package of proven maternal nutrition services is not reaching the majority of women during pregnancy. Alive & Thrive India aims to test the feasibility of integrating a package of maternal nutrition interventions in routine Reproductive, Maternal, Newborn and Child Health (RMNCH) services.These include provision of IFA and calcium supplements, interpersonal counseling on diet during pregnancy and consumption of IFA and calcium, community mobilization, and adequate weight-gain monitoring during pregnancy. This proposed evaluation aims to assess the feasibility of integrating maternal nutrition interventions into an existing RMNCH services in India, using a cluster-randomized evaluation design, complemented with a nested cohort study.

NCT ID: NCT03302949 Terminated - Tuberculosis Clinical Trials

Treating Tuberculosis Wasting With a High-protein Supplement

NUTRIATO
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Undernutrition at the time of diagnosis of active tuberculosis is a risk factor for increased mortality, and lack of weight gain during anti-tuberculous treatment has been linked to an increased relapse risk. The purpose of this study is to test the effect of Lacprodan® DI-8090 whey protein concentrate on anthropometric measures, treatment outcome and health-related quality of life, against standard practice during anti-tuberculous treatment on patients with a BMI <20 living in Guinea-Bissau.

NCT ID: NCT03240094 Completed - Aging Clinical Trials

Feasibility and Effectiveness of Nutritional Telemonitoring in Community-dwelling Elderly.

Start date: February 26, 2016
Phase: N/A
Study type: Interventional

An optimal nutritional status is essential for healthy ageing. Telemonitoring might contribute to maintaining or improving nutritional status in elderly people.The objectives of this effect study are to test the feasibility and effectiveness of telemonitoring of nutritional parameters in community-dwelling older adults.

NCT ID: NCT03211845 Completed - Aging Clinical Trials

Feasibility of Nutritional Telemonitoring in Elderly Home Care Patients

Start date: May 27, 2015
Phase: N/A
Study type: Interventional

An optimal nutritional status is essential for healthy ageing. Telemonitoring might contribute to maintaining or improving nutritional status in elderly people.The objectives of this pilot study are to test the feasibility, acceptability and implementation fidelity of telemonitoring of nutritional parameters in community-dwelling older adults; to test the study procedures for effect evaluation; and to determine the likelihood of achieving desired impact on the primary and secondary outcomes.

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: NCT02656186 Completed - Undernutrition Clinical Trials

Supplementation With Nutrients Modulating IGF-1 and Cytokines in Elderly People at Risk of Undernutrition

Start date: May 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study was to determine the improvement in nutritional status, especially in the level of insulin-like growth factor-1 (IGF-1) and its relationship with changes in the circulating cytokine levels, after providing extra protein and energy contents to community-dwelling older adults at risk of undernutrition.