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Feeding, Bottle clinical trials

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NCT ID: NCT04975282 Completed - Feeding Behavior Clinical Trials

Comparison of Bottle and Cup Feeding on Transition to Full Breastfeeding and Discharge Time

Start date: February 20, 2020
Phase:
Study type: Observational

Breastfeeding is the ideal feeding method and that in the absence of breastfeeding the bottle and cup feeding are common alternatives. There is a lack of evidence regarding superiority of either of these methods. This study aimed to evaluate bottle feeding and cup feeding in preterm infants on the outcomes of full breastfeeding and discharge time.

NCT ID: NCT04942106 Recruiting - Clinical trials for Infant, Premature, Diseases

Biobehavioral Efficacy of the Semi-Elevated Side-Lying Position

Start date: March 10, 2022
Phase: N/A
Study type: Interventional

The objective of the proposed research is to conduct a within-subject cross-over trial that will compare the efficacy of the two bottle-feeding positions on physiologic and behavioral responses of preterm infants prior to, during, and after feeding. As an exploratory aim, the investigators will also identify potential infant characteristics associated with the intervention response by evaluating infant sex, maturity level, and/or comorbidity. The two bottle-feeding positions will be the semi-elevated side-lying position (hereafter referred to as side-lying position) and the semi-elevated supine position (hereafter referred to as supine position), which is the traditional feeding position when preterm infants are bottle-fed. The investigators hypothesize that compared to the supine position, the side-lying position will be associated with greater physiologic stability in heart rate, respiratory rate, oxygen saturation, and/or autonomic nervous system regulation during and after feeding. The investigators also hypothesize that compared to the supine position, the side-lying position will be associated with more mature patterns of suck-breathe coordination and/or greater feeding skills.

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: NCT03793413 Completed - Ankyloglossia Clinical Trials

The Impact of Lingual Frenotomy on Bottle Feeding Mechanics

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

Conservative estimates show that 3-5% of all infants have tongue tie. These studies only focus on visible, anterior tongue tie. Deeper, more visibly subtle cases of ankyloglossia have not been included in these incidence numbers, so the percentage of children with ankyloglossia is much higher than previously thought. Previous research by the investigators demonstrates that posterior tongue tie can be as problematic as anterior ties. An available FDA-approved feeding solution allows for the measurement of infant sucking motions. This allows for detection of changes following surgical intervention. Previous ultrasound studies show the importance of the upward movement of the tongue, but further lingual movement parameters following frenotomy have not been reported. The primary goal of this study is to record changes in lingual movement following lingual frenotomy. The investigators plan to compare improvements over time between a control, non-intervention group and a frenotomy group. Secondary goals include recording validated outcomes of reflux and feeding efficiency.

NCT ID: NCT03655314 Completed - Breastfeeding Clinical Trials

Using the Electronic Health Record to Guide Management of Newborn Weight Loss

Start date: September 20, 2018
Phase: N/A
Study type: Interventional

Weight loss is normal for healthy newborns in the first few days, especially for those exclusively breastfed, who may have low enteral intake for several days. Although most newborns tolerate this early period of weight loss well, those with pronounced weight loss become at increased risk of feeding problems and hyperbilirubinemia, which are the two most common causes of neonatal readmission. To facilitate the assessment of risk for an individual newborn, the Newborn Weight Tool (NEWT) has been developed to categorize each infant's weight loss according to population norms, so that formula can be administered when weight loss is pronounced and avoided when weight loss is normal. The Healthy Start study will be a randomized, controlled trial testing whether displaying NEWT to clinicians providing newborn care can improve neonatal health outcomes including formula use, weight loss and readmission. Newborns will be randomly assigned either to display weight with NEWT weight categorization to their providers in the electronic health record (EHR) or to usual care (weight displayed without NEWT categorization).

NCT ID: NCT03488758 Completed - Feeding Behavior Clinical Trials

Enjoyment of Infant Formulas Based on Cow or Goat Milk Protein

CHARLIE
Start date: June 1, 2018
Phase: N/A
Study type: Interventional

To assess parental perceptions on infant feeding behavior and enjoyment with a goat milk formula compared to a cow milk formula