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Preterm Infant clinical trials

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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: 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.

NCT ID: NCT01959737 Completed - Preterm Infant Clinical Trials

Delivery Room Skin-to-skin Study

deisy
Start date: October 2013
Phase: N/A
Study type: Interventional

The first hours after birth are a sensitive period for promotion of optimal mother-child-interaction and secure attachment. Maternal sensitivity and responsivness are high in the first hours after birth due to high oxytocin levels. Developing optimal mother-child-interaction is more difficult for preterm mothers because mother and child are separated after birth and the preterm infant is not able to show strong signs to promote maternal sensitivity. We hypothesize that promoting skin-to-skin contact of VLBW infants and their mothers for 60 minutes within the first hours after birth improves mother-child-interaction at 5 to 6 months corrected age. We also hypothesize that reactivity of HPA axis and molecular patterns of stress signaling pathways differ in preterm infant with or without SSC after birth.

NCT ID: NCT01942473 Completed - Preterm Infant Clinical Trials

Effects of Automated Adjustment of FiO2 on Cerebral and Arterial Oxygenation in Preterm Infants

FiO2-Contr
Start date: August 2012
Phase: N/A
Study type: Interventional

In this study the investigators test the hypothesis that automated FiO2 adjustment increases the time of brain tissue oxygenation within the intended reference range. Furthermore, the investigators studied the change in workload during automated FiO2 adjustment as compared to manual adjustment by the nursing staff.

NCT ID: NCT01649362 Completed - Preterm Infant Clinical Trials

Effects of Prefeeding Oral Stimulation on Feeding Performance in Preterm Infants

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

The objective of this study is to evaluate the efficacy of an oral stimulation program on the length of the transition period in preterm infants (primary outcome), the length of hospital stay and the breastfeeding rates at discharge (secondary outcomes).