Clinical Trials Logo

Infant, Premature clinical trials

View clinical trials related to Infant, Premature.

Filter by:

NCT ID: NCT03225885 Completed - Premature Birth Clinical Trials

Counseling for Prematurity Using a Multimedia Education Tool

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

This study evaluates the effectiveness of prenatal counseling when verbal counseling is supplemented with a multi-media mobile application versus a written gestational age handout.

NCT ID: NCT03174301 Completed - Infant, Premature Clinical Trials

Prematurity-Related Ventilatory Control: Role in Respiratory Outcomes

Pre-Vent
Start date: March 9, 2018
Phase:
Study type: Observational

The objective of this common multicenter protocol is to test the hypothesis that algorithmic tools using clinical Neonatal Intensive Care Unit (NICU) cardiorespiratory monitoring data can detect ventilatory control instability and predict chronic and acute respiratory consequences of ventilatory control instability and autonomic dysregulation.

NCT ID: NCT03171844 Completed - Infant, Premature Clinical Trials

Early Skin to Skin in Neonatal Reanimation

PA2PRéaNice
Start date: May 31, 2017
Phase: N/A
Study type: Interventional

In the reanimation neonatal department of the Nice's hospital, 34% of newborns admitted have an umbilical vein catheter (KTVO). Their parents are admitted 24h/24h by their side, where everything is done to set up the Attachment (participation in care, skin to skin, support of breastfeeding, ...). The benefits of skin to skin described in developmental care of the newborn in the neonatal health services are well established. Nevertheless, for supposed risks (infectious and displacement of the catheter), registered in the memory of the teams, this care is not currently carried out when the newborns are carrying an umbilical venous catheter. Sometimes, because of the presence of an umbilical venous catheter, parents and their newborns could not enjoy this moment of well-being in the first days of life. We therefore propose a study evaluating the current risks of skin to skin with an umbilical venous catheter by reflecting on a new protocol for laying and fixing this medical device.

NCT ID: NCT03156946 Completed - Infant Premature Clinical Trials

Evaluation of a Peer Counseling Breastfeeding Support Program for Mother-preterm Infant Dyads

ALAIS
Start date: November 5, 2018
Phase: N/A
Study type: Interventional

Breastfeeding has a fundamental impact on the short-, medium- and long-term health of children and has an important impact on women's health. Breastfeeding protects against gastrointestinal and respiratory illnesses and is associated with better cognitive development in childhood, particularly in preterm infants. Despite these potential benefits, preterm infants experience lower rates of breastfeeding initiation and continuation compared to term infants. The use of breastfeeding peer support initiatives, in which advice is given by experienced and trained peer counselors, is an effective way to promote and support breastfeeding, regardless of a woman's socioeconomic status. Several small studies have shown that breastfeeding peer support initiatives were effective for preterm infants and that this efficacy was increased by the co-intervention of lactation consultants. The purpose of this study is to develop and to evaluate the effectiveness of a breastfeeding support program among mother-preterm infant dyads in Europe, by evaluating the impact of the intervention on 1) breastfeeding rates, 2) morbidity and mortality during the hospitalization, 3) children's cognitive development and behavior 4) mothers' mental health, 4) costs benefits. The breastfeeding support program will include peer counselors under the supervision of lactation consultants. Breastfeeding counselors will be voluntary mothers who have had a positive breastfeeding experience with at least one preterm infant. After a training course, they will meet the future or new mothers by face-to-face and share their experiences at least once a week during hospitalization and provide phone support up to 1 month after discharge from hospital. The study design will be a stepped wedge cluster trial conducted in 8 NICU in Europe (France, Switzerland and Belgium). Infants and mothers will be followed up from the time of hospitalization in the maternity and NICU up to 6 months after the discharge. The cost analysis will be performed in a subgroup of mother-preterm infant dyads that will be followed up at 24-months after their discharge

NCT ID: NCT03146351 Completed - Infant, Premature Clinical Trials

The Effects of Family Centered Intervention Program on Preterm Infants

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

Infant born preterm have an increased risk of adverse long-term developmental outcomes.The risk associated with preterm birth increase as gestational age decreases, and vulnerability remains in moderate and early preterm (<34 weeks) and late preterm (>34 weeks). There are many studies in the literature showed that the prevalence of developmental delay increases with premature birth. However, there is no study in the literature investigates effect of early intervention program motor performance in subgroups of preterm infants. Hence the aim of this study is to evaluate the differences in effects of early intervention program on motor development in early and moderate (<34 weeks) and late preterm infants.

NCT ID: NCT03136172 Completed - Hypotension Clinical Trials

Monitoring of Systemic or Organ Perfusion for Preterm Infants

Start date: May 8, 2017
Phase:
Study type: Observational

To investigate biomarker reflects systemic or specific organ perfusion well, we are going to the observational comparison study using several hemodynamic monitoring methods in the premature infants. It includes near-infrared spectroscopy (NIRS), pulse oximetry with perfusion index (PI) and pleth variability index (PVI) and functional echocardiography.

NCT ID: NCT03133663 Completed - Infant, Premature Clinical Trials

Heart Rate Evaluation and Resuscitation Trial in Preterm Neonates

HEART
Start date: June 13, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether using electrocardiograms (ECGs) during resuscitation of preterm infants (less than 31 weeks gestation) will decrease the amount of time it takes from birth for heart rate (HR) to be above 100 beats per minute and oxygen saturations to be in the goal range, in other words to stabilize the infant. A few studies have been conducted which showed that ECGs are faster at detecting HR than pulse oximetry (PO). Sample sizes, however, have been small and only few extremely low birthweight infants have been included. It is unclear if use of ECG in these tiny preterm infants in addition to traditional techniques to determine HR will be beneficial and impact resuscitation and outcomes. The investigators propose a study where infants will be randomized to either using ECG in addition to PO ± auscultation versus PO ± auscultation only to assess HR during neonatal resuscitation. The investigators hypothesize that the group of infants randomized to ECG will be able to stabilize faster, i.e. achieve HR > 100 beats per minute and oxygen saturation in goal range faster.

NCT ID: NCT03082313 Completed - Infant Development Clinical Trials

Movement-based Infant Intervention

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

The objective is to pilot test the effectiveness of an evidence-based intervention to promote positive neurodevelopmental outcomes in infants at risk for developmental delay. The intervention promotes movement experience from 3 months to sitting onset.

NCT ID: NCT03081611 Completed - Infant, Premature Clinical Trials

RAM Cannula VS Short Nasal Prongs for Delivering NIPPV in Preterm Infants

RAMCAN
Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Randomized control trial, Ram cannula VS short nasal prongs for delivering Non Invasive Positive Pressure Ventilation (NIPPV) for preterm infants

NCT ID: NCT03025815 Completed - Infant, Premature Clinical Trials

Effects of the Oral Stimulation Program in Extreme Preterm Infants

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

The purpose of this study is to determine whether oral stimulation program are effective to improve oral feeding efficiency. The sample size estimated in 74 preterm, randomized classification of the subjects into to experimental and a control group.