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Infant, Premature, Diseases clinical trials

View clinical trials related to Infant, Premature, Diseases.

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NCT ID: NCT02153736 Completed - Clinical trials for Infant, Premature, Diseases

Initial Efficacy Study of Supporting Play, Exploration, & Early Development Intervention

SPEEDI
Start date: April 2014
Phase: N/A
Study type: Interventional

The primary aims of this randomized controlled trial are to evaluate efficacy potential of SPEEDI at enhancing reaching and play based problem solving compared to infants receiving usual care.

NCT ID: NCT02101086 Completed - Clinical trials for Anemia of Prematurity

Autologous Cord Blood Transfusion in Preterm Infants

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the efficacy and safety of autologous cord blood transfusions in very-low-birth-weight premature infants, and to evaluate the developmental outcomes of the infants who received autologous transfusions.

NCT ID: NCT02085499 Completed - Clinical trials for Respiratory Insufficiency

Flow-synchronized Nasal IMV in Preterm Infants

Start date: March 2014
Phase: N/A
Study type: Interventional

The use of non-invasive methods of respiratory support to reduce complications of prolonged invasive mechanical ventilation in preterm infants has increased. The most common mode is nasal intermittent mandatory ventilation (NIMV). In NIMV, the interval between mechanical breaths is fixed and is determined by the frequency dialed by the clinician. Asynchrony between the infant's spontaneous breathing may exist since mechanical breaths delivered at fixed intervals can occur at different times over the inspiratory or expiratory phases of the infant's spontaneous breathing. Synchronized-NIMV is a mode similar to NIMV where the ventilator cycle is delivered in synchrony with the infant's spontaneous inspiration. This has been achieved by using techniques to detect the infant's spontaneous inspiration. The advantages or disadvantages of synchronized compared to non-synchronized NIMV remain to be determined. This study seeks to evaluate the effect of synchronized NIMV versus non-synchronized NIMV on ventilation and gas exchange in premature infants who require supplemental oxygen. The hypothesis is that the use of flow synchronized nasal intermittent mandatory ventilation (S-NIMV) in comparison to non-synchronized NIMV will improve ventilation and gas exchange and reduce breathing effort. The objective of the study is to compare the effect of flow synchronized-NIMV to non-synchronized-NIMV on tidal volume (VT), minute ventilation (VE), gas exchange, breathing effort, apnea and chest wall distortion in preterm neonates with lung disease.

NCT ID: NCT02027688 Completed - Feeding Behavior Clinical Trials

Feeding Progression in Preterm Infants

Start date: July 2014
Phase: N/A
Study type: Interventional

Preterm infants face many feeding challenges during hospitalization which can prolong hospitalization, raise parental anxiety and can lead to medical instability. The Feeding Progression study will randomize preterm infants to one of two currently accepted oral feeding schedules; oral feed attempts every 3 hours or every 6 hours. The study will collect data on oral feeding success, milk transfer, sucking strength, growth and medical complications.

NCT ID: NCT01982357 Completed - Clinical trials for Infant, Premature, Diseases

Measurement of Neonatal Microvascular Hemodynamics Using Non-invasive Optical Technologies

Start date: July 17, 2013
Phase:
Study type: Observational

Alterations to microvascular blood flow in premature infants, are known to contribute to several major disease entities. The optically-measured tissue blood flow, to determine tissue perfusion that can be use to detect blood loss.

NCT ID: NCT01735578 Completed - Clinical trials for Necrotizing Enterocolitis

Splanchnic Tissue Oxygenation During Enteral Feedings in Anemic Premature Infants at Risk for Necrotizing Enterocolitis

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

Necrotizing enterocolitis (NEC) is the most common gastrointestinal emergency encountered in the newborn intensive care unit and represents a significant cause of morbidity and mortality in infants born prematurely. Among possible risk factors, a strong association between elective RBC transfusions in premature infants with anemia and the subsequent development of NEC has been consistently observed (6-11). However, a significant (and increasing) number of VLBW infants with anemia are managed with erythropoiesis stimulating agents (such as Epo) and iron and do not receive RBC transfusions during their hospital stay. The present study proposes to study this particular group of VLBW infants that remain with low (<28 %) hematocrit while receiving full enteral feedings. The investigators hypothesize that significant anemia in VLBW infants will be associated with a baseline low cerebro-splanchnic oxygenation ratio (CSOR) (<0.75) as measured by NIRS, and that nasogastric feedings (NGF) in those particular patients will lead to further decreased splanchnic oxygenation. The investigators further postulate that CSOR values will be significantly lower among VLBW that develop NEC as compared to infants that do not.

NCT ID: NCT01731613 Completed - Clinical trials for Infant, Premature, Diseases

Adjustable Fortification of Human Milk Fed to Chinese Preterm Infants

Start date: August 2012
Phase: N/A
Study type: Interventional

This clinical trial will compare how the individualized and fortified human milk feeding will help a premature infant grow.

NCT ID: NCT01626508 Completed - Clinical trials for Infant, Premature, Diseases

Prospective Evaluation in Older Premature, Untreated Breast Milk and Milk Processed by the Breast-milk Bank

ADiLL
Start date: June 2012
Phase:
Study type: Observational

The purpose of this study is to evaluate the impact of the enteral nutrition type (untreated breast milk, or breast milk processed by the breast-milk bank) on the longitudinal evolution of the total content and plasma profile of essential fatty acids (EFA) in a population of premature infants.

NCT ID: NCT01539356 Completed - Neonatal Sepsis Clinical Trials

Hepcidin Levels in Preterm Infants

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

A recently isolated peptide hormone, hepcidin, is thought to be the principal regulator of iron homeostasis. Hepcidin acts by limiting intestinal iron absorption and promoting iron retention in reticuloendothelial cells. The aims of this study were to determine serum hepcidin levels in preterm infants who receive blood transfusion and preterm infants having sepsis, in order to assess possible relationships between hepcidin and serum iron, serum ferritin,in iron load situations.

NCT ID: NCT01304394 Completed - Clinical trials for Infant, Premature, Diseases

Safety During Use of Paediatric Triple Chamber Bag Formulas

Start date: February 2008
Phase: Phase 3
Study type: Interventional

The primary objective of this study was to provide daily information on the performance safety of the Ped3CB in practical therapeutic use in pediatric patients.