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Premature Birth of Newborn clinical trials

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NCT ID: NCT02023788 Completed - Clinical trials for Bronchopulmonary Dysplasia

Long-term Safety and Efficacy Follow-up Study of PNEUMOSTEM® in Patients Who Completed PNEUMOSTEM® Phase-I Study

Start date: April 2014
Phase:
Study type: Observational

This is a 5-year long-term follow-up study of open label, single-center, phase I clinical trial to evaluate the safety and efficacy of PNEUMOSTEM® in premature infants with bronchopulmonary dysplasia.

NCT ID: NCT01881256 Completed - Clinical trials for Premature Birth of Newborn

The BabyGrow Longitudinal Study of Nutrition and Growth in Preterm Infants

BabyGrow
Start date: March 2010
Phase: N/A
Study type: Observational

This is a longitudinal, observational study on nutrition, growth and body composition in preterm infants. Aims to determine the adequacy of actual nutrient intake during the preterm period by investigating associations between macronutrient supply, growth, and body composition at 34-weeks gestation, term equivalent and 2-month corrected gestational age.

NCT ID: NCT01748214 Completed - Clinical trials for Premature Birth of Newborn

Premature Infant Exposure to Noise Generated by Respiratory Support

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

Infants in neonatal intensive care units are increasing exposed to non-invasive ventilatory support modes (nasal continuous positive airway pressure - NCPAP and high flow nasal cannula: >1 L/min flow - HFNC). While there have been small descriptive studies of noise exposure in infants on NCPAP, there have been no comparative trials done comparing noise exposure in infants undergoing both NCPAP and HFNC. Objective: Using a cross-over model determine noise exposure levels in infants exposed to similar levels of respiratory support provided by NCPAP and HFNC.

NCT ID: NCT01678638 Completed - Inguinal Hernia Clinical Trials

Timing of Inguinal Hernia Repair in Premature Infants

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

The purpose of this study is to determine whether early (before NICU discharge) or late (55-60 weeks post-menstrual age) inguinal hernia repair is safer for premature infants who have an inguinal hernia.

NCT ID: NCT01628510 Completed - Clinical trials for Premature Birth of Newborn

The Developmental Effects of NICU Positioning

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

The purpose of this study is to investigate the developmental effects of two different types of positioning used with premature infants in the neonatal intensive care unit.

NCT ID: NCT01619228 Completed - Clinical trials for Premature Birth of Newborn

Skin Maturation in Premature Infants

Start date: April 2012
Phase:
Study type: Observational

The skin barrier lipids will be lower in premature infants than in full term infants and will become normal over 3-4 months after birth. The higher skin pH in premature infants will be related to an altered lipid composition which will change as the skin acidifies.

NCT ID: NCT01354028 Completed - Clinical trials for Premature Birth of Newborn

Effects of Massage Therapy to Induce Sleep in Preterm Infants

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

Premature infants sometimes require sedation to ensure minimal movement during diagnostic procedures such as MRIs. However, sedatives may produce adverse effects. The purpose of this two-day study is to determine whether massage therapy will promote sleep in preterm infants and also help them to stay asleep, providing a safer way to sedate infants for procedures. A small instrument called a sleep watch or actigraph will be placed around the infant's ankle to measure muscle activity and provide an indication of sleep. Infants will receive a 10- minute massage on one morning of the study and no massage on the alternate morning. Recordings from the actigraph will show whether there is difference in sleep pattern with and without massage. Infants will be monitored for any heart rate and oxygen saturation changes on both mornings of the study.

NCT ID: NCT01327079 Completed - Critically Ill Clinical Trials

The Use of Methadone in Newborn Infants

Methadone
Start date: December 2010
Phase: Phase 1/Phase 2
Study type: Interventional

This proposed investigation will test the following hypotheses: 1) Enzymatic activity of CYP2B6 characterized by the formation clearance of methadone to EDDP (CLf,EDDP), is directly related to both gestational and postnatal age; 2) variations in the CYP2B6 gene (SNPs) are associated with variable activity of the CYP2B6 enzyme (as measured by the formation clearance, CLf,EDDP), and 3) the elimination rate of methadone and its major metabolite EDDP in neonates is dependent on the glomerular filtration rate and therefore on the stage of development (defined by both gestational and postnatal age). The investigators propose to develop a PK model for methadone dosing in neonates that takes into account both developmental stage and genetic variability. The long-term goal of the proposed investigations is to improve dosing of methadone in neonates exposed to opioids in utero or post-natally, leading to improved control of their withdrawal syndrome and decreased adverse drug reactions associated with the current use of methadone in these vulnerable patients. More immediately, the investigators will develop a PK model for methadone dosing based on relevant developmental and genetic characteristics. The acquired knowledge based on the proposed study will lead to a more efficacious treatment of pain or opiate withdrawal syndrome in newborn infants with a decreased chance of adverse drug reactions.

NCT ID: NCT00722943 Completed - Clinical trials for Premature Birth of Newborn

Neuroendocrine Mechanisms of Developmental Massage Therapy (DMT) in Preterm Infants: Clinical Study

DMT
Start date: July 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to see if daily massage therapy will help premature infants respond to stress better, as well as improve their growth and neurobehavioral development.