Clinical Trials Logo

Premature Birth clinical trials

View clinical trials related to Premature Birth.

Filter by:

NCT ID: NCT04413994 Recruiting - Prematurity Clinical Trials

Exclusive Human-milk in Preterm NEOnates and Early VASCular Aging Risk Factors (NEOVASC)

NEOVASC
Start date: October 9, 2020
Phase: N/A
Study type: Interventional

Early vascular aging has its origins in fetal and neonatal life. The NEOVASC clinical trial aims to determine the effects of an exclusive human milk diet in extremely preterm infants on long-term cardiovascular health.

NCT ID: NCT04413019 Completed - Clinical trials for Preterm Premature Rupture of Membrane

Domiciliary Versus Hospital Management of PPROM

PPROM
Start date: April 15, 2019
Phase:
Study type: Observational [Patient Registry]

This study is designed to compare efficacy & safety of planned domiciliary versus hospital care for women with preterm prelabor rupture of the membranes (PPROM) on fetal, neonatal and maternal outcome.

NCT ID: NCT04409678 Recruiting - Preterm Birth Clinical Trials

Physical Activity and Preterm Birth With Cervical Dynamics

Start date: May 26, 2020
Phase: N/A
Study type: Interventional

this RCT is designed to investigate the influence of physical activity on the risk f preterm birth for women with cervical dynamics.

NCT ID: NCT04408807 Completed - Clinical trials for Retinopathy of Prematurity

Stress Induced by Screening for Retinopathy of Prematurity - Should Speculum and Indentation Rather be Avoided

stressROP
Start date: September 3, 2019
Phase: N/A
Study type: Interventional

The purpose is to assess the hypothesis that indirect ophthalmoscopy for retinopathy of prematurity eye examination (ROPEE) screening without the use of a lid speculum and scleral indentation (speculum-free, SpF) is less painful/stressful than funduscopy with speculum (Sp) and scleral indentation.

NCT ID: NCT04404816 Completed - Clinical trials for Respiratory Distress Syndrome

Effects of Non-invasive Ventilation With Helium-oxygen Mixture in Premature Infants With Respiratory Distress Syndrome

Start date: January 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The use of a mixture of helium with oxygen (heliox) as a breathing gas may be beneficial due to its unique physical properties, such as low density and high carbon dioxide (CO2) diffusion coefficient. In previous studies in neonates with respiratory failure, conventional ventilation with heliox was associated with improved oxygenation and selected respiratory parameters. The use of heliox may increase the effectiveness of intermittent nasal positive pressure ventilation (NIPPV), but knowledge about the effects of such therapy on newborns is limited.The use of non- invasive neurally adjusted ventilatory assist (NIV-NAVA) allows synchronization and assessment of electrical activity of the diaphragm (EaDI) during heliox administration in premature babies with respiratory failure.

NCT ID: NCT04400396 Enrolling by invitation - Prematurity Clinical Trials

Effect of Target Fortified Human Milk on the Growth Quality of Very Preterm Infants (TargetFort)

TargetFort
Start date: February 1, 2020
Phase:
Study type: Observational

It is reported that the standard method for fortification of human milk (HM) overestimates the energy and protein densities of HM (Macedo MHNP 2018), thus originating infant undernutrition (Macedo AJP 2018). The target fortification, based on analysis of HM composition, is considered the gold-standard method (Rochow 2015, McLeod 2016). This observational mixed cohort study aims to assess if very preterm infants fed HM with target fortification have greater growth during hospital stay and better body composition at term post-menstrual age (PMA), than those fed HM with standard fortification.

NCT ID: NCT04400175 Completed - Premature Birth Clinical Trials

Effects of a Valved Feeding System in Late-preterm Newborns: the Safe Oral Feeding Trial

SOFT
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

Comparing with a randomized controlled trial two different feeding systems in two groups of late-preterm newborns for evaluating which is more efficient in promoting the coordination in the process of sucking-swallowing-breathing and better cardiorespiratory stability. The B-ESP group will be fed with a feeding system with a valved ergonomic teat; the B-STD with a standard feeding system.

NCT ID: NCT04391634 Completed - Respiratory Failure Clinical Trials

Cerebral and Circulatory Effects of Neonatal Volume Targeted Ventilation

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The aim of the study was to assess the effect of volume targeted vs. pressure-controlled mechanical ventilation (MV) on circulatory parameters and cerebral oxygenation in the extremely preterm infants.

NCT ID: NCT04384328 Terminated - Preterm Birth Clinical Trials

Evaluation of an Early Support Programme in Orthophony

PAPEV-ortho
Start date: November 27, 2019
Phase: N/A
Study type: Interventional

Prospective, interventionnal with minimal risks and constraints, multicentric, non-randomized, open study, to measure the impact of an early support programme in speech and language therapy for vulnerable children (PAPEV-ortho), in children born very prematurely or very hypotrophically, on the incidence of language and communication deficits at the corrected age of 2 years.

NCT ID: NCT04383379 Recruiting - Premature Infant Clinical Trials

To Improve the Rate of Mother's Own Milk Feeding of Premature Infants in NICU

Start date: May 15, 2020
Phase: N/A
Study type: Interventional

Thirteen hospitals in China will participate in the study, which objectives of this study is to improve the rate of mother's own milk feeding of premature infants in neonatal intensive care unit(NICU), evaluate the effectiveness of improving the quality of breastfeeding in clinical use ,form standardized process and improve clinical medical quality of premature infants.