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Prematurity clinical trials

View clinical trials related to Prematurity.

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NCT ID: NCT03738293 Withdrawn - Prematurity Clinical Trials

Continuous Glucose Monitoring of Late Preterm Birth After Corticosteroids

Start date: December 2019
Phase:
Study type: Observational

Women undergoing late preterm birth are at high risk of delivering a newborn with neonatal hypoglycemia. The investigators plan to monitor interstitial glucose levels prior to delivery in these women in order to develop a better understanding of the relationship between maternal hyperglycemia and neonatal hypoglycemia.

NCT ID: NCT01805206 Withdrawn - Prematurity Clinical Trials

Prediction of NEC With Urinary iFABP

Start date: November 2014
Phase: Phase 2
Study type: Interventional

During the first four days of life, intestinal fatty acid binding protein (iFABP) is elevated in the urine of premature babies who go on to develop necrotizing enterocolitis (NEC) days to weeks later. This study aims to determine whether the withholding of feedings in babies with an elevated urinary iFABP can reduce the incidence of NEC.

NCT ID: NCT01802047 Withdrawn - Prematurity Clinical Trials

Impact of Different Electric Pumping Modalities on Milk Volume Production in Mothers of Preterm Infants

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

Initiating and sustaining breastfeeding are common challenges in neonatal units. It is known that hindmilk expressed at the end of the expression session has a higher fat content. Previous studies have shown that simultaneous pumping is more effective at producing milk than sequential pumping. However this approach is often felt uncomfortable by the mothers, and sequential pumping is preferred. The purpose of this study is to determine which modality of milk expression by electric pump is the most efficient and productive when sequential pumping is used.This is done by assessing the milk volume expressed per expression and its macronutrients content.

NCT ID: NCT01277874 Withdrawn - Clinical trials for Respiratory Distress Syndrome

Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support

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

This study will seek to enroll neonates requiring Nasal Continuous Airway Pressure (NCPAP) respiratory support and randomize them to either oscillatory (Osc-NCPAP, study group) or non-oscillatory (NCPAP, control group) mode. The goal of the research is to determine if Osc-NCPAP provides improved ventilation support compared to routine NCPAP, i.e. NCPAP without oscillations. This will be measured by need for change to ventilator support, improvement in pCO2 values, and reduction in respiratory rate and frequency of apnea during the period of NCPAP treatment. Other respiratory outcomes will also be compared, including time on NCPAP, time on High-Flow Nasal Cannula support following NCPAP, and time-averaged PiO2 from start of study to end of respiratory treatment.

NCT ID: NCT01256346 Withdrawn - Prematurity Clinical Trials

Electrocardiography Versus Pulse Oximetry for Newborn Heart Rate Determination

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

The goal of this study is to compare the time required for accurate heart rate measurement of the preterm newborn when using pulse oximetry versus electrocardiography leads.

NCT ID: NCT01121328 Withdrawn - Clinical trials for Respiratory Distress Syndrome

Autologous Umbilical Cord Blood Transfusion for Preterm Neonates

Start date: July 2011
Phase: Phase 1
Study type: Interventional

This is a pilot study to test feasibility of collection, preparation and infusion of a baby's own (autologous) umbilical cord blood in the first 14 days after birth if the baby is born premature <35 weeks of gestation.

NCT ID: NCT01050192 Withdrawn - Prematurity Clinical Trials

Nutritional Content of Breast Milk From Mothers of Premies

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

The purpose of this study is to determine the correlation, if any, between the nutritional content of breast milk pumped by the mothers of very low birth weight (VLBW) infants in the neonatal intensive care unit (NICU) and the nutritional value they are actually receiving in a 24 hour period, since as a practical matter, these may not be the same.

NCT ID: NCT00994058 Withdrawn - Prematurity Clinical Trials

Pilot Study of Electronic Uterine Contraction Inhibitor

PSEUCI
Start date: October 2009
Phase: Phase 1
Study type: Interventional

The objective is to test a novel paradigm for the inhibition of human preterm uterine contractions. The study hypothesis is that human preterm contractions can be safely inhibited with a weak electrical current provided by an electrical inhibition/uterine pacemaker device. Preterm birth is still a major problem. Current methods of preventing the uterine contractions of preterm are limited and associated with many side-effects affecting both the mother and baby. A reliable method of preventing preterm uterine contractions would be an important discovery. Such a method could eventually lead to a long-term goal of decreasing neonatal morbidity and mortality.

NCT ID: NCT00425581 Withdrawn - Hypotension Clinical Trials

N-Terminal Pro-B-Type Natriuretic Peptide and Troponin Levels as Markers of Hemodynamic Stability in Very Low Birth Weight Infants During the First Days of Life

Start date: February 2007
Phase: N/A
Study type: Observational

The primary objective is to test the hypothesis that there is an association between the hemodynamic status and the serum levels of NT-proBNP and cTnT in prematurely born infants. We would also evaluate the hypothesis that there is an association between the level of these proteins in the serum and the short and long term morbidity.