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Nutrition Disorders clinical trials

View clinical trials related to Nutrition Disorders.

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NCT ID: NCT06283342 Completed - Clinical trials for Infant Nutrition Disorders

Prophylactic Iron and Nutrition in Preventing Infant Iron Deficiency

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

This study aimed to reveal the effects of prophylactic iron preparations, adequate breast milk intake, and iron-rich supplementary food intake in the prevention of IDA (iron deficiency anemia) and ID (iron deficiency) in infancy.

NCT ID: NCT06146322 Completed - Diabetes Clinical Trials

Barley Beta-glucan, Glycemic Control, and Appetite

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

Novel barley varieties high in the soluble fiber β-glucan have the capacity to improve population health through improving glycemic control. Sweetened and unsweetened wholegrain barley foods were tested in a randomized, controlled, crossover human clinical trial to assess impact on postprandial appetite and food intake.

NCT ID: NCT06115525 Completed - Malnutrition Clinical Trials

Isolated or Combined Use of NUTRIC Score and NRS-2002 to Predict Mortality in the Intensive Care Unit

Start date: February 10, 2023
Phase:
Study type: Observational

The objective of this investigation was to assess the predictive capacity of the NUTRIC Score and NRS-2002, separately or combined, in forecasting hospital, 28-day and 3-month mortality in patients with respiratory failure admitted to the intensive care unit.

NCT ID: NCT05897892 Completed - Clinical trials for Nutrition Disorders in Old Age

The Clinical Study on the Mangrove Sword Bean Food Bar Effect for Older People

FF
Start date: August 1, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical study is to assess the api-api mangrove sword bean food bar effect on the older people's weight affected by a landslide The main questions aimed to answer are: - Can api-api mangrove sword bean food bar improve the weight of older people affected by landslide? - Can balanced nutrition education increase the older peoples' knowledge? Participants divided in the two groups i.e.: - Treatment group received 50 g mangrove sword bean food bar each day during 15 days. - Control group received 50 g sword bean food bar each day during 15 days. - Both groups obtained balanced nutrition of older people education once at the first week of study.

NCT ID: NCT05785013 Completed - Surgery Clinical Trials

The Impact of Preoperative Supplementation of Zinc

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

1. Pre operative anthropometric assessment including : weight in kg, height/length and BMI 2. Pre operative Zinc supplementation (dose according to the age) for 7 days preoperatively for cases 3. Postoperative data collection

NCT ID: NCT05777980 Completed - Nutrition Disorders Clinical Trials

Effect of Prosthetic Rehabilitation on Nutritional Status of Geriatric Patients

Start date: May 28, 2021
Phase:
Study type: Observational

This study examines the effects of prosthetic treatment options applied to edentulous geriatric individuals who applied to Marmara University Faculty of Dentistry on chewing function, food consumption status, malnutrition status and oral health-related quality of life.

NCT ID: NCT05747911 Completed - Migraine Disorders Clinical Trials

Dietary Advanced Glycation End Products and Migraine

Start date: February 1, 2022
Phase:
Study type: Observational

Is dietary intake of advanced glycation different between individuals with and without migraine? Is there a difference between the groups in terms of energy and nutrients? The answers to these questions are sought.

NCT ID: NCT05586269 Completed - Obesity Clinical Trials

Intervening in Food Insecurity to Reduce and Mitigate (InFoRM) Childhood Obesity

Start date: February 13, 2023
Phase: N/A
Study type: Interventional

The goals of this study are to 1) pilot the feasibility of a novel meal kit delivery intervention in families and children with food insecurity and obesity and 2) evaluate the implementation of the pilot intervention.

NCT ID: NCT05567211 Completed - Clinical trials for Sports Physical Therapy

Prevention of Energy Deficit Syndrome in Female Athletes. Molecular Mechanisms Associated With Malnutrition.

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

Energy Deficit Syndrome (RED-S) is the impairment of physiological functioning caused by relative energy deficiency and includes impaired metabolic rate, menstrual, endocrine, hematological, immunological, gastrointestinal, bone, psychological, developmental and cardiovascular function. Eighty-seven percent of athletes show at least one symptom related to RED-S, with a higher prevalence in women. Treatment of RED-S preferably involves a multidisciplinary team of health professionals to address the complex interaction of nutrition, training, body image and performance. The main objective is to prevent energy deficit syndrome in female athletes in the province of Alicante through different training and diet protocols using a virtual platform. A 12-week single-blind randomized clinical trial with an intervention period and a control period (RCT) is proposed. The sports federations of the most representative practices in the province of Alicante will be selected by randomized sampling. The female athletes will be randomly divided into 4 groups (control group; control group with free use of the virtual platform; intervention group with Mediterranean diet and physical exercise planning; intervention group with red fruits and physical exercise planning).

NCT ID: NCT05390437 Completed - Clinical trials for Child Nutrition Disorders

Nutritional Intervention For The Treatment Of Uncomplicated SAM

SAM
Start date: January 4, 2020
Phase: N/A
Study type: Interventional

nutritional intervention with ready to use therapeutic food (plumpy nut. by Unicef) and Prebiotics supplimentation ( Galactooligosaccarides). will be given to uncomplicated severe acute malnourished children of 06 months to 59 months of age in southern Punjab Pakistan.one group will be given Ready to use therapeutic food and placebo the other group will be given Prebiotics supplementation (Galacto oligosaccharides) with RUTF ( Ready to use therapeutic Foods).for 60 days primary out will be Mid Upper Arm Circumference >11.5 centimetre