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Premature Birth clinical trials

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NCT ID: NCT01973036 Completed - Clinical trials for Premature Rupture of Membranes

FOLCROM Trial: Foley Catheter in Rupture of Membranes

FOLCROM
Start date: March 2014
Phase: N/A
Study type: Interventional

Multicenter randomized clinical trial comparing oxytocin versus oxytocin and foley catheter for induction in women who present with premature rupture of membranes who are not in labor.

NCT ID: NCT01965769 Completed - Premature Infant Clinical Trials

Effects Of Not Measuring Gastric Residual Content On Feeding Tolerance In Premature Infants iNFANTS

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

Omitting evaluation of gastric residual contents prior to feeding very premature infants will increase the feeding intake at 2 weeks, and total caloric intake and growth by 3 weeks, as well as decrease the time required for parenteral nutrition.

NCT ID: NCT01963065 Completed - Preterm Birth Clinical Trials

NICU-HEALTH (Hospital Exposures and Long-Term Health)

Start date: March 1, 2015
Phase:
Study type: Observational

The purpose of this study is to evaluate the impact of environmental exposures during the NICU hospitalization on preterm infant development. The research team is interested in both chemical and non-chemical exposures. Research studies have shown that babies are exposed to plasticizers (bisphenol A, phthalates) in the NICU. Plasticizers are chemicals that are used to make plastic medical equipment soft and flexible. The research team wants to find out whether NICU-based exposure to chemicals (including common plasticizers) and other non-chemical exposures like stress makes a difference to how they grow and develop.

NCT ID: NCT01955135 Completed - Retinopathy Clinical Trials

Anesthesia for Retinopathy of Prematurity

Start date: September 2010
Phase: Phase 4
Study type: Interventional

Premature infants experience more respiratory problems after surgical procedures. The investigators aimed to compare general anesthesia with sedation on the need for post-operative mechanical ventilation in infants undergoing retinopathy of prematurity surgery.

NCT ID: NCT01955044 Completed - Clinical trials for Premature, Extremely Low Birth Weight Infants

PUFA Supplementation in Premature Infants

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

The purpose of this study is to determine if buccal administration of a concentrated formulation of long-chain polyunsaturated fatty acids (LCPUFA) can help to maintain docosahexaenoic acid (DHA) levels in extremely low birth weight (ELBW) infants.

NCT ID: NCT01954095 Completed - Preterm Birth Clinical Trials

The Impact of Vaginal and IM Progestins on the Cervix

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

The purpose of this study is to analyze how the body handles and responds to progesterone treatment in parous and nulliparous women at risk of pre-term birth.

NCT ID: NCT01952093 Completed - Premature Birth Clinical Trials

Effects of Early Intervention for Preterm Children at School Age

Start date: May 2013
Phase:
Study type: Observational

Despite the remarkable achievements in neonatal survival of preterm infants with very low birth weight (VLBW, birth weight < 1,500 g) over the past three decades, improvements have produced little change in their prevalence of severe developmental disability and the rate of low severity dysfunctions (e.g., learning disabilities, low IQ, attention-deficit hyperactivity disorder, specific neuropsychological deficits, poor perceptual-motor skills and internalizing behavioral problems) remains high as 50% to 70%. Few intervention programs developed for preterm infants in Western societies were shown to have short- to long-term benefits in certain cognitive functions, however, rare studies have investigated intervention effect at school age and explored plausible neurological pathway for effective intervention. This three-year study was therefore aimed to extend our previous research to longitudinally examine the effectiveness of three intervention programs (clinic-based intervention program [CBIP], home-based intervention program [HBIP] and usual care program [UCP]) for VLBW preterm children in Taiwan at seven years of age.(The intervention had been delivered from birth to one year of corrected age in the previous study. The intervention will not be given in this study.)The CBIP and HBIP contained similar child- and parent-focused services as well as interaction activities but were respectively delivered at the clinic for the CBIP and at home for the HBIP. A total of 178 VLBW preterm infants had been randomly assigned to the CBIP, HBIP or UCP. Sixty-two gender and maternal education level matched term children with normal birth weight had also been included to serve as the reference group for comparison of developmental outcomes. Effectiveness examined included child and parent outcomes. The long-term effect of the early intervention for preterm children would provide important information to help medical professionals and public policy makers to develop an effective intervention for Taiwanese preterm children who are at risk of developmental disorders.

NCT ID: NCT01946308 Completed - Clinical trials for Premature Infant Sleep

Sleep Organization in Premature Infants With Feeding Difficulties

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

Babies born too soon, premature babies, can have complications following birth because their systems are immature. Hospitals help prevent deformities and delays in motor development by using therapeutic positioning to provide containment as they would experience in the womb. They also often have trouble eating. They have discomfort, are irritable, refuse to eat and cry because their digestive system is immature. The neonatal intensive unit can create stress and disrupt their sleep. Going from active to deep sleep is essential for infant brain development, learning and memory formation. Their sleep states early in life predict their developmental outcome. The purpose is to determine whether a conformational positioning system, one that can mold to the baby and contain him or her, will allow more time asleep in premature infants with feeding problems compared to the standard crib mattress. We hypothesize that the number of total sleep time will be longer and the number of arousals out of sleep lower when they are sleeping on the conformational positioning system compared to the mattress.

NCT ID: NCT01944956 Completed - Clinical trials for Other Preterm Infants

Swallowing Sound in Preterm Infant Evaluation of Feeding Maturation

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

Our objective was to evaluate maturation of sucking and swallowing in preterm infants using a non-invasive method: assessment of swallowing sounds. Findings in healthy term infants were used as reference values.

NCT ID: NCT01942967 Completed - Clinical trials for Respiratory Distress Syndrome

Impact of Different Modes of Noninvasive Ventilation on Regional Oximetry and Hemodynamics in Premature Newborn

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

The purpose of this study is to examine the blood flow and the delivery of oxygen to the brain and gut in preterm babies while they are supported with two modes of breathing machine and compare these two methods to see if one allows for better blood flow to the brain and gut.