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Preterm Infant clinical trials

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NCT ID: NCT03151122 Not yet recruiting - Preterm Infant Clinical Trials

The Effect of a Nurse-led Continuous Support Program on Neurodevelopment of Preterm Infants

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

The objective of the study is to establish a continuous nurse-led integrated support program and to exam its impact on preterm infant neurodevelopment. Research hypotheses include:1. The continuous nurse-led integrated support will have significant impact on preterm infant neurodevelopment; 2.The support program will also have positive effect on parent psychological well-being.

NCT ID: NCT03141723 Completed - Preterm Infant Clinical Trials

Kangaroo Mother Care With Plastic Bag (Trials 2A & 2B)

Start date: May 19, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the combination of Kangaroo Mother Care (KMC) as continuously as possible together with the use of a plastic bag in combination with routine World Health Organization (WHO) thermoregulation care reduces the incidence of moderate (32-36° C) or severe (<32.0° C) hypothermia in term infants ≥ 37 0/7 weeks of gestational age (GA) when compared to KMC as continuously as possible together with routine WHO thermoregulation care.

NCT ID: NCT03140891 Completed - Clinical trials for Respiratory Distress Syndrome

Nasal High Frequency Oscillation Ventilation(NHFOV) for Respiratory Distress Syndrome

NHFOV
Start date: April 15, 2017
Phase: N/A
Study type: Interventional

In very preterm infants with severe respiratory distress syndrome(RDS), invasive ventilation(IV) , besides nasal continuous positive airway pressure (NCPAP) and early/selective pulmonary surfactant administration, is one key cornerstone to reduce neonatal mortality. However, IV is related to increased risks of bronchopulmonary dysplasia (BPD) and abnormal developmental outcomes in the survival.Weaning from IV is therefore a key procedure to reducing these risks above, and if extubation does not success, repeated intubation and/or prolonged duration of IV will result in increased medical burden and intubation-associated complications and death. How to minimize the need for endotracheal ventilation and subsequent complications constitutes a challenge for neonatologists.

NCT ID: NCT03104946 Completed - Preterm Infant Clinical Trials

To Research the Relation Between Neonatal Morbidities and Poor Outcome in Preterm Infants

Start date: September 1, 2013
Phase: N/A
Study type: Observational

From November 2014 to October 2015, a multi-centers retrospective study was conducted to collect compliance, and 8 three-level hospitals from China were included. The infants survived to a postmenstrual age of 36 week with birth weight less than 1500g and without congenital disease. The birth weight, gestational age, morbidities and poor outcomes( death, cerebral palsy, cognitive, et al) were recorded. Data were analyzed with Chi-square test to observe the relationship between morbidities and poor outcomes. And the predictive effect on the number of the top three morbidities were analyzed by Logistic regression analysis.

NCT ID: NCT03064022 Completed - Preterm Infant Clinical Trials

Preterm Infant Multicentre Growth Study

PreMGS
Start date: February 2009
Phase:
Study type: Observational

The purpose of this study is to improve health professionals understanding of preterm infant growth patterns, and to determine if early growth patterns predict risks of adverse metabolic and cognitive outcomes.

NCT ID: NCT02837276 Completed - Acute Kidney Injury Clinical Trials

Intermittent Hypoxemia and Acute Kidney Injury Study (IHAKI Study)

IHAKI
Start date: July 2016
Phase:
Study type: Observational

This pilot study aims at investigating the relationship between intermittent hypoxemia (IH) and acute kidney injury (AKI) in preterm infants. AIM 1: Test the hypothesis that intermittent hypoxemia is associated kidney injury in preterm infants, as reflected by a rise in serum creatinine. AIM 2: Test the hypothesis that there is rise in acute kidney injury urinary biomarkers with increased intermittent hypoxemia.

NCT ID: NCT02811432 Completed - Preterm Infant Clinical Trials

Kangaroo Mother Care Before Stabilisation Amongst Low Birth Weight Neonates in Africa

OMWaNA
Start date: October 13, 2019
Phase: N/A
Study type: Interventional

We will conduct an individually randomised, controlled, superiority trial with two parallel groups; an intervention arm allocated to receive KMC and a control arm receiving 'standard' care. The primary aim is to examine the impact of KMC initiated before stabilisation on mortality within 7 days relative to standard care amongst neonates ≤2000g at four hospitals in Uganda. We hypothesise that neonates in the arm allocated to receive KMC before stabilisation will have a 25% overall reduction in mortality within 7 days compared to neonates allocated to receive standard care.

NCT ID: NCT02528851 Not yet recruiting - Preterm Infant Clinical Trials

Cardiorespiratory Effects of "Higher" Versus "Equivalent" CPAP Upon Extubation From High EAP in Preterm Infants

CO-PAP
Start date: October 2015
Phase: N/A
Study type: Interventional

The aim of this study is to compare the cardiovascular and respiratory effects of "higher" versus "equivalent" CPAP pressures post-extubation from high endotracheal airway pressures (EAP), defined as at least 8 cm H2O (water), in the form of a randomized controlled cross-over trial. Endotracheal airway pressure (EAP) will be defined as mean airway pressure (MAP) [if on high frequency ventilation] or positive end-expiratory pressure (PEEP) [if on conventional ventilation] at time of extubation. Participants will be randomized to "higher" CPAP group (CPAP level 2cm H2O higher than the extubation EAP) or "equivalent" CPAP group (CPAP level equal to the extubation EAP) before undergoing crossover to the other arm. We hypothesize that "higher" CPAP levels, when compared to "equivalent" CPAP levels, do not adversely impact the cardiorespiratory status when a patient is extubated from high EAP.

NCT ID: NCT02496104 Recruiting - Preterm, Infant Clinical Trials

Habituation's Mechanisms in Preterm and Term Infants

HABIPREMA
Start date: July 9, 2015
Phase:
Study type: Observational

Each year in France, 7 % of newborns are born preterm (before 37 weeks of gestational age (GA)). The investigators called very preterm infants those who were born before 33 weeks of GA. These very preterm infants have a higher risk of developing neurological complications like developmental disabilities or cerebral palsy. To date, early assessment of these infants is difficult and not reliable enough to detect those who are at risks of developing neurological issues. Now, the investigators need to identify earlier these infants to provide them interventions to improve their development (physical therapy for example). Consequently, the investigators are examining a study whose aim is to assess preterm infants habituation. Habituation is the newborn ability to become familiar with new environmental stimulations (noise, light…). This habituation allows the newborn to maintain his sleep even at onset of a noise or light. To study this phenomenon in infants born preterm near to corrected term (around 40 weeks of postnatal GA), will allow us to better understand neurological development of these infants. The investigators plan to compare habituation skills of preterm infants near to their theorical date of birth (40 weeks of GA) to a population of infants born at term. The investigators will also study the link between habituation abilities and sleep quality as well as neurodevelopmental outcome at the corrected age of two years old.

NCT ID: NCT02024828 Completed - Preterm Infant Clinical Trials

Testing Four Feeding Approaches to Oral Feeding in Preterm Infants

PRO
Start date: July 2006
Phase: N/A
Study type: Interventional

The purpose of this study was to test the effect of four randomly assigned approaches to oral feeding transition on feeding outcomes in preterm infants.