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Children clinical trials

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NCT ID: NCT01666548 Completed - Children Clinical Trials

Haemolytic Uraemic Syndrome in Childhood: Clinical, Cognitive and Psychological Aspects

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

The purpose of this study is to investigate the clinical, cognitive outcome and psychosocial outcome of haemolytic uraemic syndrome in childhood. The haemolytic uraemic syndrome (HUS) is the leading cause of acute renal failure in childhood. The more common typical HUS is mostly caused by Shigatoxin-producing enterohaemorrhagic Escherichia coli (EHEC). The rarer atypical HUS is mainly caused by different genetic abnormalities in complement regulatory proteins. About 50 till 60 percent of all patients with HUS develop a severe acute renal failure and require dialysis. Resulting from new diagnostic and therapeutic approaches the survival rate increased during the last years. Despite this, there are only few data concerning long-term prognosis, cognitive and motoric development, as well as psychological coping and health-related quality of life of affected children and their parents.

NCT ID: NCT01658267 Completed - Children Clinical Trials

Compliance With Dietary Recommendations in Children at Risk for Undernutrition

Start date: October 2011
Phase: Phase 3
Study type: Interventional

This study will assess compliance with dietary recommendations, in conjunction with a nutritional supplement to meet the nutritional requirements in children and the effects of the compliance on promoting growth in children who are at risk of under-nutrition.

NCT ID: NCT01652287 Completed - Children Clinical Trials

Safety of BB-12 Supplemented Strawberry Yogurt For Healthy Children

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

The investigators believe a readily available drink containing a high dose of probiotics has the potential to improve compliance through many of these mechanisms. This product also has the potential to positively impact the health of children and adults around the world, as yogurt will likely be more appealing to both children and their parents for long term consumption than pharmaceutical-like preparations. In addition to the benefits associated with the consumption of probiotics, there is an increased health benefit from consuming yogurt, a nutrient dense food. More specifically, the rationale for this Phase I study is to determine safety of this yogurt drink and comply with FDA recommendations pertaining to an Investigational New Drug application. The investigators hypothesize that BB-12 is safe in generally healthy children ages 1-5 years.

NCT ID: NCT01618929 Completed - Children Clinical Trials

Effects of Montelukast in Asthmatic Children With and Without Food Allergy

Start date: March 2013
Phase: Phase 4
Study type: Interventional

- To search the effects of montelukast on the airway inflammation including FEV1%, FEV1%/FVC, the provocholine® (methacoline chloride powder for inhalation) challenge tests, the leukotriene levels in the exhaled breath condensate in asthmatic children with and without food allergy aged 6-18 years old. - To define the patient groups with good response to montelukast and to define the parameters which predict the good response.

NCT ID: NCT01541033 Completed - Autism Clinical Trials

Biomarker of Children With Familial Autoimmune History

Start date: November 2009
Phase: N/A
Study type: Observational

The purpose of this study is to identify biomarkers in this subset of autism patients, design a protein based assay system for screening serum for these biomarkers and confirm that these serum antibodies are still present at one year's time.

NCT ID: NCT01538706 Completed - Neoplasms Clinical Trials

Hospital-based Home Care for Children With Cancer

Start date: August 2008
Phase: N/A
Study type: Interventional

The purpose of this non-randomized controlled intervention study was to evaluate the effects of a hospital-based home care program for children with cancer at a university hospital in Denmark. The hypothesis was that hospital-based home care could replace an out-patient visit or an in-patient admission without increasing the incidence of adverse events and costs. Furthermore, to enhance the children's quality of life and the psychosocial impact on the family.

NCT ID: NCT01515254 Completed - Children Clinical Trials

The Feeding Dynamic Intervention: Self Regulation of Intake in Preschoolers

FeeDIn
Start date: February 2012
Phase: N/A
Study type: Interventional

In this study the investigators will examine the Feeding Dynamic Intervention (FDI) as a tool to prevent obesity in young children. The purpose of the intervention is to improving caregiver feeding practices, child eating behaviors, and child self-regulation of energy intake in the short term.

NCT ID: NCT01449656 Completed - Children Clinical Trials

A Comparison of the Laryngeal Mask Airway (LMA) Proseal and LMA Supreme in Children

Start date: October 2011
Phase: N/A
Study type: Observational

The aim of this randomized prospective study is to compare two laryngeal mask airways with a provision for evacuation of gastric contents, the LMA Proseal and The investigators hypothesize that airway leak pressures with the LMA Proseal will be significantly different (higher) when compared with the LMA Supreme.

NCT ID: NCT01413594 Completed - Cerebral Palsy Clinical Trials

Bimanual Training in Children With Hemiplegia

HABIT
Start date: July 2011
Phase: N/A
Study type: Interventional

A randomized control trial of bimanual training in children with hemiplegia. The protocols have been developed at Columbia University to be child friendly and draws upon our experience since 1997 with constraint-induced movement therapy in children with cerebral palsy. The investigators will test the hypothesis that bimanual training (HABIT) will result in improved hand function in children with hemiplegia.

NCT ID: NCT01409785 Completed - Children Clinical Trials

A Comparison of the LMA Unique and LMA Supreme in Children

Start date: August 2011
Phase: N/A
Study type: Observational

The goal of this study is to compare the LMA Unique and LMA Supreme in children having surgery. We hypothesize that the airway leak pressures with the LMA Supreme will be superior to the LMA Unique. Airway leak pressures will be measured by recording the circuit pressure at which equilibrium is reached. The ease of placement, fiberoptic grade of laryngeal view, feasibility of use, and complications (airway related, gastric insufflation, trauma) will also be assessed.