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Preterm Birth clinical trials

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NCT ID: NCT01766908 Completed - Preterm Birth Clinical Trials

Optimal Timing of Cord Clamping in Preterm Pregnancy Following Vaginal or Cesarean Delivery

CordClamp
Start date: December 2012
Phase: N/A
Study type: Interventional

This is an experimental research study for pregnant women between 23 and 37 weeks age of gestation who will be having a baby sooner than term. This study is to learn if waiting 20, 40, or 60 seconds to clamp the umbilical cord after baby delivers will improve his/her outcome and overall health. Benefit to the baby may come by increasing the amount of blood in the baby's body, reducing the need for possible transfusion later, and possible prevention of other complications caused by too little blood in the baby. Possible reduction of cerebral palsy may be realized by a longer interval for cord clamping.

NCT ID: NCT01753843 Completed - Preterm Birth Clinical Trials

Brief Delay in Cord Clamping and Neurobehaviour in Preterms

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

RESEARCH HYPOTHESIS Brief delay(>30 sec to <60 sec ) in cord clamping as compared to early cord clamping (< 20 sec) leads to a better short term neurobehavioural outcome in preterm (34-36 wks) neonates when assessed by neurobehavioral assessment of preterm infants (n.a.p.i.) at 37 weeks of post conceptional age

NCT ID: NCT01683565 Completed - Preterm Birth Clinical Trials

Preemie Tots: A Pilot Study to Understand the Effects of Prematurity in Toddlerhood

Start date: September 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine whether supplementation with certain polyunsaturated fatty acids can help development and behavior of children born preterm.

NCT ID: NCT01648855 Completed - Preterm Birth Clinical Trials

Consequences of Antiangiogenic Factors Involved in Preeclampsia on Intra-uterine Growth Restricted Preterm Newborn

ANGIODYS
Start date: June 2012
Phase: N/A
Study type: Observational

Preeclampsia complicates about 2-7% of pregnancies and is a major contributor to maternal and neonatal morbidity and mortality worldwide. Imbalance between circulating angiogenic and antiangiogenic factors has emerged as a potential key pathway in the pathophysiology of preeclampsia. Patients with preeclampsia have a higher circulating concentration of antiangiogenic factors (ie, soluble vascular endothelial growth factor receptor-1 [sVEGFR- 1], also called soluble fms-like tyrosine kinase 1 [sFlt1]) and soluble endoglin (sEng)] and a lower maternal circulating concentration of free angiogenic factors (ie, vascular endothelial growth factor [VEGF] and placental growth factor [PlGF]) than patients with a normal pregnancy. Bronchopulmonary dysplasia is the main respiratory sequelae of preterm birth. Its rate increased in preterm infants born from mother with preeclampsia. Recent studies showed that bronchopulmonary dysplasia is consistently accompanied by a reduction in the number of small arteries and on abnormal distribution of vessels within the distal lungs. This is associated with reduced lung VEGF expression. The main objective of this population-based study, ie in intra uterine growth restricted preterm babies born before 30 weeks of gestational age, was to examine whether levels of sFlt1 at birth in maternal and umbilical cord blood and in the amniotic fluid is associated with an increased risk of BPD.

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.

NCT ID: NCT01576783 Completed - Preterm Birth Clinical Trials

Omega Tots: A Randomized, Controlled Trial of Long-chain Polyunsaturated Fatty Acid Supplementation of Toddler Diets and Developmental Outcomes

Start date: April 26, 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine whether supplementation with certain polyunsaturated fatty acids can help the cognitive development of children born preterm.

NCT ID: NCT01523483 Completed - Preterm Birth Clinical Trials

Vaginal Progesterone for Prevention of Preterm Birth After an Episode of Preterm Labor

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

The investigators study objective is to investigate the effectiveness of vaginal micronized progesterone in prolonging pregnancy after an episode of preterm labor which responded to tocolytic treatment. Furthermore, the investigators aim is to study the mechanisms of actions of progesterone supplementation by examining its effect on the two components of parturition: cervical ripening and myometrial contractility. The investigators will utilize transvaginal ultrasound to assess the changes in the cervical tissue, and non-invasive trans-abdominal uterine EMG to assess the uterine muscle activity. The investigators will also look at the effect of progesterone on contraction frequency by tocodynamometer (TOCO), though EMG is expected to provide much more information.

NCT ID: NCT01487824 Completed - Preterm Birth Clinical Trials

What is the Impact of Early Life Exposures on the Cardiovascular System in Young Adulthood?

EVS
Start date: May 2007
Phase:
Study type: Observational

The purpose of this study is to investigate whether early life exposures such as premature birth or exposure to preeclampsia before you are born results in long-term alterations in the cardiovascular system that increase risk of cardiovascular disease development.

NCT ID: NCT01460576 Completed - Preterm Birth Clinical Trials

Improving Prematurity-Related Respiratory Outcomes at Vanderbilt

IMPROV
Start date: September 2011
Phase: N/A
Study type: Observational

The goal of IMPROV is to identify molecular mechanisms that contribute to lung injury and long-term breathing problems in preterm infants by investigating two interrelated biochemical pathways: the urea cycle-nitric oxide pathway and the glutathione pathway. The investigators hypothesize that prematurity-related limitations in the function of these important biochemical pathways contribute to respiratory disease risk over the first year of life.

NCT ID: NCT01436786 Completed - Preterm Birth Clinical Trials

Effectiveness of Guided Imagery Intervention on Factors Associated With Maternal Stress and Preterm Birth

Start date: June 2010
Phase: N/A
Study type: Interventional

Demonstrating the effectiveness of an economical and feasible intervention such as guided imagery on factors associated with preterm birth, along with better understanding of pathways leading to adverse birth outcomes has tremendous health, social, and financial benefits. This project has the potential to significantly advance the field of nursing and knowledge development in the areas of maternal stress reduction in African American women and to provide scientific evidence of the effectiveness of guided imagery.