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Premature Birth clinical trials

View clinical trials related to Premature Birth.

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NCT ID: NCT00722085 Completed - High Risk Pregnancy Clinical Trials

Amniotic Fluid Sludge in Cerclage Patients as an Indicator for Increased Risk of Preterm Delivery and Neonatal Outcome.

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

Amniotic Fluid "Sludge" Does Not Increase Risk of Preterm Delivery in Cerclage Patients.

NCT ID: NCT00718705 Completed - Prematurity Clinical Trials

Reduction of Spontaneous Prematurity by Antibiotic Treatment (Josamycin)

PREMYC
Start date: July 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the effectiveness of an antibiotic treatment (Josamycin) in the case of positive PCR for Ureaplasma spp. and/or Mycoplasma hominis in the second quarter on the risk of premature birth.

NCT ID: NCT00711633 Completed - Clinical trials for Preterms With Gestational Age Ranging From 30 to 35 Weeks

Evaluation of Safety, Tolerance and Effects on the Intestinal Flora of a New Fermented Milk for Preterm Infants

Start date: December 2002
Phase: N/A
Study type: Interventional

The intestinal flora is a complex ecosystem which is known to play various important functions in the gut. Recent data have reported a delay in intestinal colonization in preterm. Modulating the intestinal flora through dietary supplementation with probiotics or prebiotics has been shown to improve digestive and general outcomes in full-term infants.The aim of this study was to evaluate the clinical tolerance, the effect on gut microbiota, and the mucosal inflammatory responses to a fermented milk in preterm infants.

NCT ID: NCT00707837 Completed - Preterm Infants Clinical Trials

Nutritional Study in Preterm Infants

Start date: May 2005
Phase: Phase 3
Study type: Interventional

An evaluation of a preterm infant formula containing ingredients similar to those found in breastmilk

NCT ID: NCT00706264 Completed - Preterm Birth Clinical Trials

Prevention of Preterm Birth Using Cervical Pessary in Pregnant Women With Short Cervix

PECEP
Start date: June 2007
Phase: N/A
Study type: Interventional

Placement of a vaginal pessary reduces significantly the rate of spontaneous preterm birth in pregnant women with short cervical length at 18-22 weeks scan.

NCT ID: NCT00701350 Completed - Preterm Birth Clinical Trials

Biomarkers of Intra-amniotic Infection in Women With Preterm Premature Ruptured Amniotic Membranes

PPROM
Start date: June 2008
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the expression of protein biomarkers in cervical vaginal fluid in women with preterm premature rupture of membranes (PPROM)

NCT ID: NCT00689676 Completed - Prematurity Clinical Trials

Expressive Language and Cognitive Early Development in Very Low Birth-Weight Preterm Toddlers

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

The aim of the present study is to describe the performance of very low birth-weight preterm toddlers regarding expressive language and cognitive development during sensorimotor and beginning of pre-operational periods, as well as to compare the performance presented by these children to that presented by their full-term peers, according to Genetic Epistemology theoretical principles. The hypothesis of this study is that very-low birth weight preterms would present a poorer performance, concerning expressive language and cognition development,than their full-term peers.

NCT ID: NCT00684697 Completed - Clinical trials for Neurodevelopmental Outcome

Iron Status and Myelination in Premature Infants

Piron
Start date: May 2009
Phase: N/A
Study type: Interventional

Premature infants with iron deficiency if supplemented with more elemental iron than the routine 2mg/kg/day will have improved brain development.

NCT ID: NCT00681018 Completed - Premature Infants Clinical Trials

Feeding Study in Premature Infants

Start date: September 2008
Phase: N/A
Study type: Interventional

To evaluate weight gain of preterm infants fed fortified human milk.

NCT ID: NCT00676247 Completed - Premature Birth Clinical Trials

Cerebral Blood Flow Parameters and Neurobehavioral Development in Infants at Term Age

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

Although several studies have contrasted the hemodynamics of cerebral arteries using cranial Doppler ultrasound between full-term and preterm infants, the assessments were mostly conducted in the first days of life. Furthermore, the clinically significant hemodynamic parameter has been established from a small sample of infants that its validity on other populations remains unclear. Therefore, the purpose of this study is twofold: 1. to examine the hemodynamics of cerebral arteries in full-term and very low birth weight preterm infants at term age 2. to assess the validity of the hemodynamic parameters in relation to concurrent neurobehavioral function. This study will enroll normal full-term infants and very low birth weight preterm infants who have no major neonatal disease. Cranial Doppler ultrasound examination will be performed on all infants at term age. Hemodynamic parameters will include peak systolic velocity, end diastolic velocity, resistance index and pulsatility index for the bilateral anterior cerebral arteries and middle cerebral arteries. Neurobehavioral development will be administered on the same day using the Neonatal Neurobehavioral Examination- Chinese version.