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Growth Failure clinical trials

View clinical trials related to Growth Failure.

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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: 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.