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Failure to Thrive clinical trials

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NCT ID: NCT01603368 Completed - Sepsis Clinical Trials

Prophylactic Probiotics to Extremely Low Birth Weight Prematures

PROPEL
Start date: June 2012
Phase: Phase 2
Study type: Interventional

Mortality and incidence of severe complications is still high among extremely premature infants. Common causes of severe complications in this population are poor nutrition, necrotizing enterocolitis, and severe infections. Feeding intolerance is also a common problem resulting in prolonged need for intravenous lines and poor nutrition. The aim of the study is to evaluate whether supplementation with the probiotic bacterium Lactobacillus reuteri DSM 17938 daily to premature infants with extremely low birth weight increases feeding tolerance to breast milk and thereby improves nutrition, increases growth and reduces serious complications and mortality in this population. Beyond this, possible mechanisms underlying these effects will be analyzed in stool, breast milk and blood samples.

NCT ID: NCT01475357 Completed - Clinical trials for Congenital Heart Defects

Intestinal Function in Neonates With Complex Congenital Heart Disease

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

Postnatal intestinal function in cardiac infants. The overall goal of this proposal is to address a widespread health problem in the pediatric cardiac infant population - poor postnatal growth - through a collaborative effort between pediatric cardiology, cardiothoracic surgery, neonatology, microbiology, and immunology. The hypothesis is that term neonates with complex congenital heart disease (CHD) who receive trophic breastmilk feeds in the pre-operative period will show improved gut function than neonates who were strictly NPO (nothing by mouth) in the pre-operative period.

NCT ID: NCT01424696 Completed - Cystic Fibrosis Clinical Trials

Baby Observational and Nutritional Study

BONUS
Start date: December 2011
Phase: Phase 2
Study type: Observational

Cystic fibrosis (CF) is a life-shortening disease that causes breathing and digestive problems, but can now be diagnosed at the time of birth. Lung function is very hard to measure in infants, but growth is not. In this study the investigators aim to define growth in infants with CF in the first year of life with research quality precision and to understand factors that interfere with good growth. Pancreatic enzyme replacement therapy (PERT) will be also be studied in a subgroup of infants. Two different doses of PERT will be evaluated for improving fat and nitrogen absorption in infants with CF.

NCT ID: NCT01371825 Completed - Clinical trials for Lysosomal Acid Lipase Deficiency

Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of Sebelipase Alfa in Children With Growth Failure Due to Lysosomal Acid Lipase Deficiency

Start date: May 4, 2011
Phase: Phase 2/Phase 3
Study type: Interventional

This was an open-label, repeat-dose, intra-participant dose-escalation study of SBC-102 (sebelipase alfa) in children with growth failure due to lysosomal acid lipase (LAL) Deficiency. Eligible participants received once-weekly (qw) infusions of sebelipase alfa for up to 5 years.

NCT ID: NCT01338363 Completed - Pneumonia Clinical Trials

Drug Utilization and Safety Events Among Children Using Esomeprazole, Other Proton Pump Inhibitors or H2-receptor Antagonists

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

The purpose of this study is 1. To describe patient characteristics and drug usage among children that are prescribed esomeprazole for the first time and to compare them with patients who are prescribed other proton pump inhibitors (PPIs) or H2-receptor antagonists for the first time. 2. To ascertain all incident hospitalized cases of angioneurotic oedema, pneumonia, gastroenteritis, failure to thrive, convulsions/seizures, acute interstitial nephritis and thrombocytopenia among new users in the three cohorts of esomeprazole, other PPIs and H2-receptor antagonists.

NCT ID: NCT01070173 Completed - Clinical trials for Idiopathic Short Stature

Ghrelin Levels in Children With Poor Growth

Start date: January 2008
Phase: N/A
Study type: Observational

The investigators hypothesize that low serum ghrelin levels may characterize a group of patients with poor weight gain and/or linear growth who do not have any other identified cause for growth failure. These patients may present with a variety of complaints and are often evaluated by both pediatric endocrinologists and pediatric gastroenterologists. The investigators hypothesize that ghrelin has a physiologically important role in linear growth and that chronic diseases of the gastrointestinal system, such as H. Pylori infection or celiac disease, may alter serum ghrelin levels in children. Low ghrelin levels may be a factor leading to poor growth, potentially by altering growth hormone secretion and/or by decreasing appetite. By measuring ghrelin levels in children with short stature and in children with gastrointestinal disease, the investigators will further elucidate the possible physiologic role of ghrelin in childhood growth and how it may be altered in conditions causing short stature and in certain gastrointestinal diseases.

NCT ID: NCT01034735 Completed - Clinical trials for Growth Hormone Deficiency

r-hGH Liquid Multidose Versus Freeze-dried Multidose Bioequivalence Trial

Start date: July 2008
Phase: Phase 1
Study type: Interventional

The primary objective of the trial was to assess the bioequivalence for two concentrations (5.83 mg/mL and 8 mg/mL) of the new r-hGH liquid multidose formulation using the r hGH freeze-dried multidose formulation (Saizen® 8 mg, 8.8 mg/1.51 mL) as reference. Each volunteer received three r hGH treatments, with each treatment being administered as a single subcutaneous dose of 4 mg r-hGH in a randomized sequence with at least one week of wash-out period between successive treatments.

NCT ID: NCT00483691 Completed - Failure to Thrive Clinical Trials

Trial of Home Visitation Among Infants With Failure To Thrive

FTT
Start date: January 1989
Phase: N/A
Study type: Interventional

1. Children in the home intervention group will have better growth (increase in weight and height) than children in the control group. 2. Children in the home intervention group will have better behavior than children in the control group. 3. Children in the home intervention group will have better academic performance than children in the control group.

NCT ID: NCT00325611 Completed - Stroke Clinical Trials

Multidisciplinary Inpatient Palliative Care Intervention

Start date: April 2002
Phase: N/A
Study type: Interventional

Palliative care is believed to improve care of patients with life-limiting illnesses. This study evaluated the impact of a multi-center randomized trial of a palliative care team intervention on the quality and cost of care of hospitalized patients. Study subjects were randomized to intervention or usual care. At study end, patients receiving the palliative care intervention reported greater patient satisfaction with their care. Intervention patients also had significantly fewer ICU admissions and lower total costs for care 6 months past their hospitalization. Intervention patients completed more advance directives and had longer hospice stays.

NCT ID: NCT00190658 Completed - Failure to Thrive Clinical Trials

Somatropin Treatment in Patients With SHOX Deficiency and Turner Syndrome

Start date: February 2000
Phase: Phase 3
Study type: Interventional

This clinical trial will compare the mean first year height velocity of somatropin-treated prepubertal patients with SHOX deficiency with the height velocity of a control group of untreated prepubertal patients with SHOX deficiency. Both groups will be compared to a somatropin-treated group of girls with Turner syndrome. After the second year patients in the control group have the option to receive treatment as well. All patients will optionally be treated until they achieved adult height.