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NCT ID: NCT01986036 Active, not recruiting - Healthy Clinical Trials

The Acute, Synergistic Effects of Protein and Calcium on Appetite and Energy Intake

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

High-protein meals have previously been shown to acutely reduce appetite and energy intake. More recently, meals higher in calcium have also been shown to increase feelings of fullness, circulating insulin and intestinal peptide concentrations and reduce appetite sensations. This study aims to assess whether calcium and protein act synergistically to acutely influence appetite and energy intake.

NCT ID: NCT01967238 Active, not recruiting - Healthy Clinical Trials

An Open Label Study of IgG Fc Glycan Composition in Human Immunity

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

In order to produce better more effective vaccines, it is important to understand the particulars of why individuals have an effective or ineffective immune response to vaccination. We are going to examine specific aspects of the antibody (IgG Fc glycan) made by healthy volunteers who receive different vaccines or who have a viral infection to understand the nature of an effective (or less effective) vaccine response. The results of this research could be used to develop adjuvants to increase/ improve vaccine response.

NCT ID: NCT01901770 Active, not recruiting - Healthy Clinical Trials

The Parents in Appalachia Receive Education Needed for Teen Project

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

This clinical trial studies an educational intervention for parents and providers in increasing human papillomavirus (HPV) vaccination rates in younger girls in Ohio Appalachia. Educational interventions may be effective in increasing the number of participants whose daughters receive HPV vaccination.

NCT ID: NCT01898026 Active, not recruiting - Healthy Clinical Trials

Soluble Fibre Enriched CHO Food Study

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

The proposed study will examine the effects of incorporating a soluble fibre blend into commonly consumed refined carbohydrate foods on sensory parameters and postprandial blood glucose. A sensory evaluation will be conducted in phase I to asses for differences between the control and fibre enriched samples of white bread, mashed potatoes, muffin, hot breakfast cereal. Phase II will be investigating the postprandial blood glucose responses of the 8 test foods from phase I.

NCT ID: NCT01897168 Active, not recruiting - Healthy Clinical Trials

Bone Mineral Content in Healthy Children

Start date: June 2013
Phase:
Study type: Observational

The primary purpose of this study is to determine the effects of early diet on bone health.

NCT ID: NCT01889056 Active, not recruiting - Healthy Clinical Trials

Non-erythroid Effects of Erythropoietin on Cognitive Function and Exercise Capacity in Humans

Start date: February 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The blood hormone Erythropoietin (Epo) is not only produced by the kidneys but also by the brain, especially under hypoxic conditions. It has been shown in animal studies and human studies that Epo has neuroprotective properties. Furthermore, there is scientific evidence for central modulatory effects of Epo in the brain but high dose of Epo is needed to overcome the blood brain barrier. In a double blind placebo controlled crossover study we will investigate the effects of a single high dose of Epo on cognitive function and exercise capacity in healthy subjects. The subjects will receive a single high dose of Epo (60.000 IU) and will perform a computerized cognitive test battery, a breathing test, a maximal exercise capacity test (VO2max), and a time trial (TT) 24 hours after the treatment. The primary outcome of the study will be the cognitive function. - Trial with medicinal product

NCT ID: NCT01883700 Active, not recruiting - Healthy Clinical Trials

Acute Vascular Response To Meals Varying In Glycemic Index And Glycemic Load

HILO
Start date: August 2010
Phase: Phase 2
Study type: Interventional

This study examines the effects of carbohydrate type (high- or low-Glycemic Index (GI)) and amount (high- or low-Glycemic Load (GL)) have on blood glucose levels, blood pressure and arterial stiffness in healthy individuals. It will also determine whether subjective ratings such as test meal palatability and hunger are related to changes in blood glucose. The investigators hypothesize that: (1) High-GI meals, regardless of GL, will increase arterial stiffness; low-GI meals, regardless of GL, will have a neutral or lowering effect on arterial stiffness (augmentation index). (2) High-GI meals, regardless of GL, will have an elevating effect on both central and peripheral blood pressures. (3) The incremental area under the curve for blood glucose will show most significant differences between high-GI, high-GL and low-GI, low-GL meals at 30 and 90 min.

NCT ID: NCT01845272 Active, not recruiting - Healthy Clinical Trials

Pharmacokinetic Interactions of Candesartan Cilexetil and Amlodipine Besylate

CCA
Start date: April 2013
Phase: Phase 1
Study type: Interventional

This study is designated to evaluate the pharmacokinetic interactions of candesartan cilexetil and amlodipine besylate in healthy male volunteers.

NCT ID: NCT01817127 Active, not recruiting - Healthy Clinical Trials

Elucidation of Breast Milk Composition and Structure Over the First Year of Lactation: UC Davis Lactation Study

Start date: April 1, 2009
Phase:
Study type: Observational

This observational study is designed to determine how sugars, lipids and proteins in breast milk vary among mothers; is affected by maternal diet, health and microbiota and vary over the course of lactation. Additionally, the study is designed to determine how the structure and composition of complex milk sugars, maternal health status and diet influence the development and maintenance of infant gut microflora.

NCT ID: NCT01736020 Active, not recruiting - Healthy Clinical Trials

Developing Anesthesia as Post Traumatic Stress Disorder (PTSD) Therapy

Start date: September 2009
Phase: Phase 1
Study type: Interventional

This preclinical phase 1 development study in healthy volunteers seeks to identify if low doses of commonly used non-triggering anesthetic agents might have clinical utility for modulating emotional memory processing and to understand the nature of the brain mechanisms of drug action. Optimally, a drug, dose and brain mechanism of action will be identified that will form the foundation for future use in clinical studies of patients with PTSD.