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Infant clinical trials

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NCT ID: NCT02366780 Completed - Infant Clinical Trials

Breast Milk Content Expressed Manually Compared to Electric Pump

Start date: November 2012
Phase: N/A
Study type: Interventional

Breast milk is a unique and unmatched nutritional and non-nutritive source of bioactive factors for the health and development of infants.Colostrum, which is produced in low quantities for the first 3 to 4 days after birth, is rich in immunologic components and developmental factors. Breastfeeding difficulties during the first days of life of an infant are common. Moreover, not all infants can be directly fed at the breast. Therefore, breast milk feeding at this early stage is initiated and promoted by the expression of breast milk either manually or by use of a pump. Whether the method of milk expression at this stage has a qualitative impact on colostrum is currently unknown. The purpose of this randomized controlled study is to compare the effect of manual expression with electric pump expression upon the macronutrient composition of breast milk.

NCT ID: NCT01573871 Completed - Infant Clinical Trials

Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula

Start date: February 2012
Phase: Phase 3
Study type: Interventional

The objective of the study is to assess gastrointestinal tolerance and compliance in infants who require a hydrolyzed formula.

NCT ID: NCT01289808 Terminated - Infant Clinical Trials

Reduced Infant Response To A Routine Care Procedure After Glucose 25% Analgesia

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

Glucose has analgesic and calming effects in newborns. To date, it is not known whether the beneficial effects extend to care giving procedures that are performed after painful procedures. The investigators objective is to determine the effect of glucose 25% analgesia for procedural pain on infant pain responses during a subsequent care giving procedure.

NCT ID: NCT01216709 Completed - Infant Clinical Trials

Iron Absorption From Infant Formula and Iron Drops in Infants (MJAU-studien)

MJAU
Start date: October 2010
Phase: N/A
Study type: Interventional

Iron deficiency (ID) affects up to 25% of Swedish infants and severe ID is associated with cognitive and behavioral problems. To avoid this, iron supplements or iron-fortified infant foods are recommended for infants. However, the optimal iron dose and mode of delivery have not yet been established. This is a concern as excessive iron intake may impair growth and increase morbidity in iron-sufficient infants. Previous studies have suggested that iron-fortified foods may have different effects than iron supplements. In this study, the investigators will investigate whether the mode of iron administration (supplementation vs. fortification) and the amount consumed (high intakes vs. low intakes) affect iron absorption, iron utilization, and zinc absorption in healthy term non-iron-deficient 6-month-old infants.

NCT ID: NCT01167270 Completed - Obesity Clinical Trials

The Intervention Nurses Start Infants Growing on Healthy Trajectories (INSIGHT) Study

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

This study will test an intervention program designed to provide developmentally appropriate guidance to parents of infants on responsive parenting and healthy lifestyle to see if that intervention will prevent rapid weight gain in infancy and overweight at age 3 years. Further, compared with control infants, intervention infants will have lower body mass index (BMI) percentiles at age 3. The investigators also hypothesize that control infants will gain weight more rapidly over time.

NCT ID: NCT01162798 Completed - Growth Clinical Trials

Preterm Infant Growth

Start date: September 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to assess growth of preterm infants fed a test formula compared to a standard formula up to the first 4 months of corrected gestational age.

NCT ID: NCT01147601 Recruiting - Infant Clinical Trials

Topical Timolol 0.5% Solution for Proliferating Infantile Hemangiomas

Start date: March 2010
Phase: Phase 0
Study type: Interventional

The purpose of this study is to learn about a new potential use for topical timolol 0.5% aqueous solution that may help treat small uncomplicated infantile hemangiomas. This study would examine whether topical timolol could be a potential therapy.

NCT ID: NCT01131663 Recruiting - Infant Clinical Trials

Design and Development of an Infant's Oriented Face Mask

Start date: April 2010
Phase: N/A
Study type: Observational

Face masks are used for many respiratory care applications such as anaesthesia, resuscitation, and aerosol therapy. None of the currently available face mask for infants and young children are specifically designed and developed for infants. The aim of this study is to design, develop and test the first infant's oriented face mask. To achieve this ultimate goal we will first define appropriate sizes of infants' faces that would be used as templates for the design and development of optimally fitted model masks. In the next stage we will use these masks and incorporate the infants' own soother (pacifier) into a new SootherMask (SM). In the last part of the study we will compare acceptance levels between Soothermask (SM) and a conventional commodity masks without a pacifier.

NCT ID: NCT01090726 Completed - Intubation Clinical Trials

Intubation With Storz Videolaryngoscope® Versus Airtraq® - in an Infant Population

Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of the pilot study is to compare new laryngoscopes for infants by assessing the equipment best suited to assist the intubation, with the best overview, shortest time to intubation and use these numbers to make a sample size calculation for the full protocol. The investigators hypothesis is that the Storz videolaryngoscope® has a better success rate than infants (<2 years). The patients will be optimally anaesthetized with neuromuscular blockade for the intubation. All patient will be evaluated with af Macintosh blade laryngoscope, with an Airtraq® or a Storz videolaryngoscope®, and finally intubated with the other one of the later, which the patient was randomized to.

NCT ID: NCT00969189 Terminated - Anesthesia Clinical Trials

Evaluation of the Pediatric Igel Airway in 250 Children

Start date: August 2009
Phase: N/A
Study type: Observational

Once a child has been anaesthetised and is fully asleep, a special airway tube called a laryngeal mask is often inserted into their mouth to help with their breathing. This tube is removed just before the child wakes up. A new type of airway tube, called an i-gel airway, has been developed for children, which is hoped will be easier to insert, safer once in position, and will be less likely to cause a sore throat after the anaesthetic than a standard laryngeal mask. The adult i-gel airway has been available for adults since 2007, and early trials have shown very encouraging results.