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Other Preterm Infants clinical trials

View clinical trials related to Other Preterm Infants.

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NCT ID: NCT02404623 Completed - Asthma Clinical Trials

The Effect of Vitamin D Administration to Premature Infants on Vitamin D Status and Respiratory Morbidity

Start date: April 2015
Phase: N/A
Study type: Interventional

This trial objective is to assess whether doubling the daily intake of vitamin D improves serum vitamin D levels and serves as primary prevention of respiratory infections and asthma in premature infants. This is a prospective randomized (1:1) double-blinded trial. The study population will be randomized into two groups (1:1): - Intervention Group - 800 IU of Vitamin D once daily - Control Group - 400 IU of Vitamin D once daily Patients will be followed up for one year after randomization for serum Vitamin D levels and respiratory morbidity.

NCT ID: NCT02268968 Completed - Clinical trials for Other Preterm Infants

Use of Topical Lidocaine to Reduce Pain in Preterm Infants Receiving Nasal CPAP Continuous Positive Airway Pressure

Start date: October 2013
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to evaluate the relative efficacy of topical lidocaine on reducing pain associated with the application of nasal CPAP in preterm infants

NCT ID: NCT02231801 Completed - Clinical trials for Other Preterm Infants

Monitoring of Vital Signs During Skin-to-skin Holding by Mothers of Their Preterm Babies

Start date: September 2014
Phase: N/A
Study type: Observational

This observational study aims to monitor the vital sign changes in both mother and baby that occur during kangaroo care in preterm infants and to investigate any potential correlations between maternal measurement values and those of the infant. The purpose of this observational study is to look for a method to track the earliest responses that could, theoretically, be considered as 'social responses' in hopes of providing developmental interventions earlier to at-risk infants.

NCT ID: NCT02192996 Completed - Clinical trials for Other Preterm Infants

Probiotic Supplementation to Improve the GUT Microbiota of Very Low Birth Weight Preterm, a Pilot Study

Start date: December 2012
Phase: Phase 0
Study type: Interventional

This pilot trial is designed to investigate the benefits of the use of probiotics in GUT microbiota development and/or immunological biomarkers and how this can be related with the clinical status of very low birth weight preterms during their first weeks of life at the neonatal intensive care unit(NICU).

NCT ID: NCT02073071 Completed - Clinical trials for Other Preterm Infants

Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weight Infants

Start date: May 2014
Phase: N/A
Study type: Observational

This is a two stage open-label, single-arm, multicenter and observational study.

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: NCT01450436 Completed - Clinical trials for Other Preterm Infants

Impact of Preterm Body Composition at Discharge on 2 Years Neurological Development (ASQ Evaluation)

EPIPOD
Start date: September 2011
Phase:
Study type: Observational

Neonatal nutritional management consists in reproducing miming uteri growth kinetic. Since the seventies, NICU (Neonatal Intensive Care Unit) strategy consists in a high proteidic input (apport) supposed to allow optimal neurodevelopment. However, nutritional practices and strategies have significantly evolved during these last years, influenced by Baker nutritional imprinting concept (2002). Actually, neonatal high proteidic exposition could perturb metabolism and hormonal systems of newborns conducting to a reinforcement of obesity and cardio-vascular pathology prevalence in this target population at adulthood. In this context many studies emerged since 2000 and try to assess the trade-off between neurodevelopment and growth under nutrition conditions. EPIPOD try to focus the link between heterogenous proteic input dispensed in our NICU (described by tercil methods on population) and fat mass phenotype variations at discharge (described by tercil methods); and its consequences on neurodevelopmental growth. Understanding how particular nutritional exposition could determine "fatty" phenotype and impact neurodevelopment is clearly our main goal.

NCT ID: NCT00233324 Completed - Premature Birth Clinical Trials

Surfactant Positive Airway Pressure and Pulse Oximetry Trial

SUPPORT
Start date: February 2005
Phase: Phase 3
Study type: Interventional

This study compared the use of continuous positive airway pressure initiated at birth with the early administration of surfactant administered through a tube in the windpipe within 1 hour of birth for premature infants born at 24 to 27 weeks gestation. In addition, these infants within 2 hours of birth, had a special pulse oximeter placed to continuously monitor their oxygen saturation in two different target ranges (85-89% or 91-95%). This study helped determine whether or not these two management strategies affect chronic lung disease and survival of premature infants.