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Premature Birth clinical trials

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NCT ID: NCT01646463 Completed - Premature Birth Clinical Trials

Pilot Trial of CenteringPregnancy With Mindfulness Skills

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

In the U.S., rates of preterm birth and low birth weight have increased over the past 30 years. Poor birth outcomes are especially high among racial/ethnic minority populations. Maternal stress is an important factor that can lead to negative birth outcomes. Thus, programs that reduce stress during pregnancy could improve birth outcomes. Initial pilot work tested a mindfulness-based approach to stress reduction during pregnancy. Women in the pilot study had lower stress and improved coping after the program. For the current study, mindfulness is added to an existing prenatal healthcare program called CenteringPregnancy (CP). CP provides prenatal care through 10 group sessions. This study compares CP with a version of CP infused with mindfulness skills training. Effects of the two versions of CP on psychological stress and coping, stress hormones, and birth outcomes will be tested. Data will be collected from participants three times: twice during pregnancy and once after birth. Medical records will provide data on birth outcomes and other health factors. The study will provide initial information about a mind-body program to reduce stress and improve birth outcomes. Data from the study will inform the development of an R01 proposal for a larger study. The study will also help advance the long term goal of reducing health disparities.

NCT ID: NCT01645137 Completed - Prematurity Clinical Trials

Effectiveness Of Osteopathic Manipulative Treatment In NICU: A Multicenter Clinical Trial

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

The use of complementary and alternative medicine in neonatal ward has been steadily rising during the last decade. This integrated medicine approach has been shown to be helpful to improve neonatal health care. Osteopathic manipulative treatment (OMT) has been applied to premature infants to reduce the length of stay and to cope with clinical complications. Results from previous studies documented the positive association between OMT and shorter period of hospitalisation as well as improvement of clinical conditions. The aim of this nationwide multicenter study is to demonstrate the effect of OMT on length of stay (LOS) in premature infants across 3 neonatal intensive care units (NICU).

NCT ID: NCT01643980 Completed - Clinical trials for Early Onset of Delivery Before 37 Weeks

Prevention of Preterm Birth in Pregnant Women at Risk Identified by Ultrasound: Evaluation of Two Treatment Strategies

PESAPRO
Start date: August 2012
Phase: Phase 4
Study type: Interventional

The preterm birth is considered as a main problem in the modern obstetrics, being the responsible of greatest of 50% neonatal morbimortality and heavy costs. Despite the significant medical advances, the rate of prematurity has not declined over the past 40 years and even continues to rise in the developed countries. In order to decrease the prematurity is necessary that two premises: to identify the pregnant women at risk of preterm birth, and dispose of useful measures aimed at prolonging the pregnancy and therefore avoid preterm delivery. The investigators propose a clinical trial with the objective to identify effective strategies to reduce the premature birth (34 weeks and earlier) rate in the population of pregnant women at risk for premature birth, which will be identified by ultrasound during the second trimester of their pregnancy. The investigators intend to compare two accepted strategies: administration of progesterone (vaginally) or the placement of vaginal pessaries. These 2 strategies are affordable, easy to apply, and they present very few maternal-fetal secondary effects.

NCT ID: NCT01643057 Completed - Clinical trials for Apnea of Prematurity

Stochastic Resonance Mattress (Physiological Interventions) and Biomarkers for Enhancing Neonatal Health

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

The purpose of this study is to explore physiological interventions and biomarkers for Apnea of Prematurity in newborn infants.

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: 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: 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: NCT01607216 Completed - Clinical trials for Bronchopulmonary Dysplasia

Functional and Lymphocytic Markers of Respiratory Morbidity in Hyperoxic Preemies

Start date: August 2011
Phase:
Study type: Observational

This is an observational study that proposes to collect clinical, physiological, cellular and molecular information in an attempt to identify a set of factors that may predict the risk for persistent lung disease in babies born prematurely.

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: NCT01601886 Completed - Preterm Birth Clinical Trials

Delivery Room Practice Change Following the Initiation of the NICHD SUPPORT Trial

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

This study was designed to analyze whether initiation of the NICHD Neonatal Research Network SUPPORT trial was followed by a change in frequency of endotracheal intubation the delivery room in non-participants and whether these changes were associated with changes in management and outcomes. The investigators hypothesized that the investigators would observe following the initiation of the SUPPORT trial a 33% reduction in the rate of intubation in the delivery room among non-participants preterm infants at Parkland Memorial Hospital.