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Malnutrition clinical trials

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NCT ID: NCT02242539 Completed - Malnutrition Clinical Trials

Tools to Improve Parental Recognition of Developmental Deficits in Children

Start date: September 2014
Phase: N/A
Study type: Interventional

In this study, we aim to improve child nutrition by increasing parents' awareness of their children's physical growth. We use a cluster-randomized trial design to evaluate two interventions that provide parents with regular information on their children's physical development and growth: 1) distribution of full-sized growth charts for measurement of child height within households; and 2) organization of community-based meetings, during which children's height and weight are measured by trained project staff.

NCT ID: NCT02241746 Completed - Malnutrition Clinical Trials

Malnutrition in Chinese Hospitalized Patients and Optimizing the Usage of Nutritional Screening Tools

Start date: August 2012
Phase: N/A
Study type: Observational

The purpose of this study is: - to diagnose malnutrition in Chinese hospitalized patients with four nutritional screening tools: mini-nutritional assessment - short form, subjective global assessment, malnutrition universal screening tool and nutritional risk screening 2002. - to optimize the usage of nutritional screening tools based on data-mining methods.

NCT ID: NCT02232113 Completed - Inflammation Clinical Trials

Frequent Dosing of CERA Improves Nutrition and Inflammation in Hemodialysis Patients

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The response of Continuous Erythropoietic Receptor Activator (CERA) with different dose interval and the survey for influence factors: We aim to evaluate a better clinical response which can be achieved by different dosing interval of a fixed dose of CERA. We expect this study can determine the dosing schedule with better clinical response to CERA and identify the associated factors predicting the cost-effectiveness of CERA in maintenance hemodialysis (HD) patients in Taiwan.

NCT ID: NCT02213393 Completed - Undernutrition Clinical Trials

Cater With Care Effect Study

CwC
Start date: October 2014
Phase: N/A
Study type: Interventional

The objective is to study the effectiveness of supplementing a standard hospital and 12-week home menu with protein-enriched Cater with Care products in reaching a protein intake of 1,2-1,5 g/kg body weight/day and in improving functional status after hospital stay in elderly patients.

NCT ID: NCT02208635 Completed - Clinical trials for Nutritional Deficiency

Absorption of Zinc (Zn) From Zn-biofortified and Zn-fortified Maize in Young Zambian Children Between 24-36 Months

HPZM
Start date: October 2012
Phase: N/A
Study type: Interventional

The objective of this study is to compare the quantity of Zn absorbed from an accurately weighed quantity (~100 g) of minimally milled control maize (~15 µg Zn/g maize), from biofortified maize (~30 µg Zn/g) and from the same control maize that has been fortified (total level of ~60 µg Zn/g) when fed to young children age 24-36 months whose major habitual food staple is maize.

NCT ID: NCT02208622 Completed - Clinical trials for Nutritional Deficiency

Bioavailability of Zinc and Iron From a Whey-based Protein Supplement Consumed With a Habitual Plant-based Diet

Start date: August 2013
Phase: N/A
Study type: Interventional

Bioavailability of iron and zinc from habitual plant-based diets consumed by young children in Mexico is low due to the high phytate content. Whey protein has been found to increase zinc absorption, thus, providing a whey based supplement with micronutrients may be an effective strategy to increase iron and zinc bioavailability from plant-based foods and alleviate iron and zinc deficiencies. The investigators compared absorption of zinc and iron in children receiving diets with and without whey protein supplements (WPS).

NCT ID: NCT02208609 Completed - Clinical trials for Nutritional Deficiency

Zinc Bioavailability From Amaranth-enriched Maize Tortillas

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

Young children in Guatemala are at risk for nutrient deficiencies due to plant-based diets and poor sanitation. Stunting, frequent diarrhea, and respiratory infections are common. Supplementation of Zn to children during diarrhea episodes has been shown to diminish duration and severity of illness. Poor Zn absorption due to high fiber and phytate in this diet might play a role in these processes. Supplementation of this micronutrient in the diet might be beneficial. The investigators will compare absorption of Zn from white maize tortillas enriched with 20% amaranth to traditional white corn tortillas in preschool children in Guatemala.

NCT ID: NCT02208531 Completed - Clinical trials for Moderate and Severe Undernutrition

Transition to Scale of Nutrition and Psychosocial Stimulation Program for Malnourished Children

TTS Bangladesh
Start date: February 2014
Phase: N/A
Study type: Interventional

We hypothesize that it is feasible to integrate a program of Nutritional Care and Pychosocial Stimulation into the Community Clinics in Bangladesh and thereby improve malnourished children's growth and development after a year of intervention.

NCT ID: NCT02200198 Completed - Surgery Clinical Trials

Respiratory Muscle Training in Malnourished Patients Undergoing Abdominal Surgery

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

Malnutrition affects 50% of hospitalized patients around the world and causes changes in respiratory muscles predisposing the development of pulmonary complications probable, because of the ineffectiveness of cough. How the training of respiratory muscles can improve the effectiveness of cough, malnourished patients could benefit from this train however, the training of the muscles in malnourished patients has not been tested for safety or efficiency. So, the aim of this study is to assess the safety and efficiency of respiratory muscle training to improve the potency of cough in malnourished patients.

NCT ID: NCT02192892 Completed - Malnutrition Clinical Trials

Acceptability Among Children and Caregivers of Amylase Porridges

AMY-01
Start date: June 2014
Phase: N/A
Study type: Interventional

Addition of α-amylase is considered as one of most effective solution to improve energy density of cereal based porridges (WHO, 2008). By adding α-amylase, the viscosity of porridges will be decreased while keeping dry matter content constant. Potential positive impact is to significantly improve efficiency of WFP nutritional programmes targeting vulnerable groups suffering from acute malnutrition. The acceptance of porridges made with α-amylase is tested compared to porridges made without α-amylase among 12-36 months old children and their caregivers. Acceptance is measured based on energy intake. The porridges tested consist of fortified blended Supercereal (12- <24 months) and Supercereal-Plus (24-36 months) based on Corn Soy Blend (CSB) extruded or drum dried, Wheat Soy Blend (WSB), Rice Soy Blend (RSB), all with and without α-amylase, or a commercial porridge, or eeZee bar.