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Preterm Birth clinical trials

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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.

NCT ID: NCT01412931 Completed - Preterm Birth Clinical Trials

Protein and Ultrasound Indicators of Preterm Birth

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

Women are being asked to participate in a research study that is looking for new methods to understand and predict premature birth (birth before 37 weeks of pregnancy—full term pregnancy is 40 weeks). In this study the investigators will be looking at proteins in vaginal fluid, tissue from the placenta after the baby is born (fetal membranes), and a new form of ultrasound of the mouth of the womb (cervix) that measures its length, volume, and stiffness, in order to try to know who will have a preterm birth and who will reach full term. The investigators will collect the vaginal fluid samples and perform ultrasounds both in the clinic throughout pregnancy in normal women, and from women admitted to the hospital because they are in early labor. The investigators will collect the placental tissue after the baby is born (this is normally discarded). This study will help us to understand the process of preterm birth and the investigators hope that this will eventually allow us to develop better methods to treat preterm labor and prevent the birth of premature babies.

NCT ID: NCT01380158 Withdrawn - Preterm Birth Clinical Trials

Preventing Preterm Birth With a Pessary

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

The primary objective of this study, is to determine the effect of a Cup pessary, a device that is currently readily available in the USA and similar in design to the Arabin pessary, on the incidence of delivery prior to 37 weeks in women with a history of prior spontaneous birth (before 37 weeks) and incidentally found to have a cervix less than 25 mm in length prior to 23 weeks.

NCT ID: NCT01371019 Completed - Preterm Birth Clinical Trials

Proteomic Assessment of Preterm Birth

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

The purpose of this study is to to collect and store blood samples that will be utilized to develop a multimarker test to predict preterm delivery.

NCT ID: NCT01355536 Completed - Diabetes Mellitus Clinical Trials

Metabolic and Endocrine Status in Women With Prior Preterm Birth

Start date: October 2006
Phase: N/A
Study type: Observational

The prevalence of preterm birth is rising in most western countries. The causes of preterm birth is not fully understood and seem to be multifactorial. The endocrine and metabolic aspects are scarcely investigated.The main purpose of this study is to test the hypothesis that endocrine and metabolic factors associate to preterm births.

NCT ID: NCT01348230 Withdrawn - Preterm Birth Clinical Trials

Glycoproteomic Analysis of Urine in Women Undergoing Spontaneous Preterm Delivery

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

When babies are premature, or born before they are fully developed, they face many different medical problems, some of which are quite devastating, such as cerebral palsy, mental retardation, blindness, deafness, severe intestinal problems, and developmental delays. Unfortunately, in more than half the cases of premature births, there is no procedure or test that an obstetrician can employ to predict if a fetus is at risk for premature birth, especially when the mother is healthy. This study seeks to determine if certain factors found in the urine undergo specific changes that can be used to detect premature births of this type before they happen.

NCT ID: NCT01344616 Completed - Preterm Birth Clinical Trials

Reducing Preterm Births in Underserved Pregnant Women

Start date: August 2010
Phase: Phase 2
Study type: Interventional

Timely screening and management of modifiable conditions can reduce preterm births, yet providing effective prenatal risk management systems to meet the unique needs of medically underserved populations is complex. If the proposed system proves to be effective in reducing preterm births it can improve maternal and child quality of life as well as reduce the economic burden of preterm births in the U.S.