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Infants clinical trials

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NCT ID: NCT06447558 Completed - Infants Clinical Trials

The Effects of "Oral Administration of Breast Milk Droplets" and "Palatal Stimulation With a Finger"

Start date: May 1, 2021
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the effects of "oral administration of breast milk droplets" and "finger palatal stimulation" on feeding tolerance in preterm neonates fed with orogastric tube feeding. This randomized controlled experimental study was conducted in the neonatal intensive care unit of a private hospital. The study included 90 premature newborns born at 28-36 weeks of gestation and admitted to the intensive care unit. The intervention group consisted of 60 infants and the control group consisted of 30 infants. "Demographic Information Form" and "Patient Follow-up Form" were used to collect data. Data collection tools were used before, during and after the procedures in all groups. In one of the intervention groups, breast milk droplets were applied to the oral cavity of the newborns, and in the other group, the palate of the newborns was stimulated using a finger. These interventions were performed for 5 minutes every 3 hours for 7 days during the newborns' feeding times. Neonates in the control group were fed with an orogastric tube by following hygiene rules, but no study intervention was performed in these infants. SPSS (Statistical Package for Social Sciences) 22.0 for Windows software was used for statistical analysis.

NCT ID: NCT05492253 Completed - Clinical trials for Healthy Participants

First Complementary Foods and the Infant Gastrointestinal Microbiota

Start date: January 30, 2023
Phase: N/A
Study type: Interventional

This study evaluates the effect of different complementary foods on the gastrointestinal microbiota of exclusively human milk fed infants.

NCT ID: NCT04598841 Completed - Clinical trials for Hirschsprung Disease

Nutrition Support for Hirschsprung Disease

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

A multi-center, prospective,randomized, non-blind, controlled study was conducted to investigate the effects of different pre-operative nutritional support modes on perioperative nutritional status, surgical treatment success rate, and rehabilitation process in children with Hirschsprung disease.

NCT ID: NCT04218929 Completed - Newborn Clinical Trials

Evaluation of Growth, Safety, and Efficacy of an Infant Formula for Healthy Term Infants

Start date: December 10, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate that a new infant formula for term infants supports age-appropriate growth. This study is designed in accordance with Good Clinical Practice guidelines and the requirements of the Code of Federal Regulations, 21CFR106.96. In this randomized, controlled trial (RCT), healthy, term, formula-fed (FF) infants will be randomized to one of two infant formulas: a standard, commercially-available infant formula for term infants (CF) or the study formula for term infants (SF) for 16 weeks. A reference group of human milk-fed infants will also be enrolled. The primary efficacy objective is to compare the growth of infants randomized to the study infant formula (SF) versus growth of infants randomized to the standard commercial infant formula (CF).

NCT ID: NCT03716882 Completed - Infants Clinical Trials

Acoustic Structures Crying of Infants From 1 to 4 Months and Their Signification

LongCRY
Start date: October 16, 2018
Phase:
Study type: Observational

Crying is a survival mechanism for babies and their almost exclusive means of expression until the age of 4 months. Babies 'cry is mostly related to pain, a feeling of hunger, discomfort or separation following the departure of a parent around. Crying is a complex but essential means of communication and information between a baby and his parents that raises the question of their meaning. The cry phenomenon consists of complex acoustic signals produced by the vocal cords and filtered by the vocal tract. The vibrations frequency determines the fundamental frequency, itself responsible for the perception of the cry tone (pitch). The frequency spectrum of a cry is modified during the passage through the upper airways forming broad bands called "resonance frequency" or "formants". From the specificity of a crying sequence, it is possible to extract dynamic information and relate it to the perception that the adult has of it. Thus dynamic crying is often perceived by the adult as an imminent need of the baby. Some studies have shown that a child's crying may change according to his degree of discomfort, suggesting that crying was a "graduated signal" whose frequency and timbre could vary along a continuum. These changes would explain why adult listeners would be able to dissociate crying babies of different intensities. Conversely, an inappropriate response to crying could gradually generate disorders of the relationship between the baby and the parent. However, despite their potential neuro-ethological interest, knowledge of information transmitted by babies's cry remains superficial. This could be related to the relatively obsolete techniques of recording or due to the lack of objective physiological data on babies 'cry. Finally, the perception and reactions of adults when they hear crying babies are not fully understood.

NCT ID: NCT03327415 Completed - Infants Clinical Trials

Nutri-Bébé 2013 Survey on Food Consumption of Infants and Young Children

NBB2013
Start date: January 3, 2013
Phase: N/A
Study type: Observational

The Nutri-Bébé 2013 survey is an observational cross-sectional study aiming to update food consumption, practices and nutrient intakes in children under 3 years of age in metropolitan France.

NCT ID: NCT02119104 Completed - Infants Clinical Trials

Prevenar (13v) Infant Drug Use Investigation

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

The purpose of this study is to investigate post marketing use and safety of Prevnar ( 13v) in infants vaccinated for the first time at the age of 2 months, inclusive, to 7 months, exclusive.

NCT ID: NCT01664234 Completed - Difficult Airway Clinical Trials

Oxygen Insuflation and ArterialDesaturation During Tracheal Intubation in Children

Start date: January 1, 2012
Phase: N/A
Study type: Interventional

Infants (0-1 yr.) with anticipated difficult airways will be enrolled in the study. Specifically, we will include infants with cleft palate, Pierre Robin, Treacher Collins, trisomy 21, or similar congenital malformations. Patients with American Society of Anesthesiologists physical status scores ≥3 will be excluded, as will those with congenital heart disease and left-to-right shunting. Patients will be randomly assigned to laryngoscopy with or without simultaneous insufflation of oxygen at 4 L/minute. Oxygen will be provided by a flowmeter connected via rigid tubing to the track-mounted endotracheal tube on the AirTraq. Randomization (1:1) will be based on computer-generated codes with random block sizes and stratified by hospital; allocation will be concealed and provided to clinicians via a secure web site that will be accessed shortly before induction of anesthesia.