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Growth clinical trials

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NCT ID: NCT05405738 Completed - Growth Clinical Trials

Cleft Palate Technique and Maxillary Growth

Start date: May 6, 2022
Phase:
Study type: Observational

comparison of the maxillary growth between cleft palate patients that underwent to repair by 2 flap palatoplasty versus Furlow with buccinator technique

NCT ID: NCT05302427 Completed - Growth Clinical Trials

Infant Massage and Infant Growth, Mother-Infant Attachment, and Maternal Self-Confidence

Start date: November 29, 2021
Phase: N/A
Study type: Interventional

Touch is an essential element in the healthy growth and development of the baby. Infant massage is the best way to touch babies. In line with the literature review on the subject, it has been reported that infant massage supports growth and development in infants, improves attachment between mothers and babies and decreases the level of depression and anxiety in mothers. With the coronavirus pandemic, quarantine decisions have been implemented all over the world. In addition to the stress brought on by their new roles, new mothers have to cope with the anxiety and stress of being a parent and babysitting during the pandemic period. During the pandemic process, it is seen that depression and anxiety levels increase in mothers who have given birth, and maternal attachment is negatively affected. Depression and anxiety in mothers negatively affect the cognitive, physical, social and emotional development of babies. It is very important to encourage practices that increase mother-infant interaction, such as infant massage, during the pandemic period. The universe of the research will consist of mothers and their babies who were followed up in İzmir Karşıyaka No. 8 Gülay Kaymak Family Health Center and Karşıyaka No. 4 Bostanlı-2 Family Health Center between May 2021 and May 2022. The sample of the study is 38-42. It is planned to create babies born in the 4th week of pregnancy, with a birth weight of over 2500 grams and who have completed their fourth week (one month old) (n:60).

NCT ID: NCT05150288 Completed - Growth Clinical Trials

Human Milk Oligosaccharides (HMOs) Post-market Study on Infants (NEHMO)

NeHMO DACH
Start date: July 8, 2019
Phase: N/A
Study type: Interventional

Human milk oligosaccharides (HMOs) represent the third largest solid component of breast milk. Technology advancements made it possible to supplement infant formulas with HMOs (2'FL, LNnT). Two published RCTs have demonstrated that infant formulas supplemented with 2'FL or 2'FL+LNnT are safe, well-tolerated, support normal grow, and may support healthy GI function and confer immune benefits. The performance of HMOs-supplemented formulas assessed in a real-world setting is complementary to previously conducted RCTs conducted in highly controlled clinical settings. Main objectives will be to monitor the safety & tolerance of HMOs-supplemented formulas in larger and diverse infant populations; to assess the performance of HMOs-supplemented formulas in mixed-fed infants, a population that was not studied in previous RCTs but likely represents a relatively common feeding regimen. Finally, considering the potential health/immune benefits of HMOs, it is also important explore the incidences of illnesses (i.e., respiratory illnesses, GI illnesses, and fever) associated with consuming HMOs-supplemented formulas and compare with breastfed infants data.

NCT ID: NCT05117164 Not yet recruiting - Death Clinical Trials

Enteral Feeding in Infants With Duct Dependant Lesions.

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

This is a multicenter randomised controlled trial to assess whether standardised enteral feeding in newborns with duct dependenty congenital heart disease decreases the risk of necrotising enterocolitis (NEC). The investigators plan to include a total 384 infants. The study will be carried out in three level III hospitals in Poland. The primary end will be NEC and/or death. Secondary end points include weight gain, hospital length of stay, time required to reach full feeding.

NCT ID: NCT05047978 Completed - Growth Clinical Trials

Growth and Tolerance of a Partially Hydrolyzed Infant Formula

Start date: August 28, 2021
Phase: N/A
Study type: Interventional

The purpose of this research study is to compare the growth and tolerance of infants who consume either an infant formula with intact proteins or an infant formula with partially hydrolyzed proteins through approximately 12 months of age.

NCT ID: NCT04957992 Active, not recruiting - Growth Clinical Trials

Infant Formula and Toddler Drink Feeding Study

Start date: July 21, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the growth and development outcomes of infants fed a new infant formula and toddler drink through 24 months of age.

NCT ID: NCT04766346 Completed - Growth Clinical Trials

Nutritional Supplementation in Children Aged 1-3 Years Experiencing Growth Concerns

Start date: February 26, 2021
Phase: N/A
Study type: Interventional

This open-label clinical trial will gain evidence of the effect of an oral Nutritional Supplement (NS) to help improve catch-up growth and support learning skills in children with growth concerns.

NCT ID: NCT04736082 Completed - Growth Clinical Trials

Safety of an Infant Formula With Hydrolysed Protein in Term Infants

HASI
Start date: March 16, 2021
Phase: N/A
Study type: Interventional

A multi-centre, randomised, double-blind, parallel-group, controlled, prospective, non-inferiority intervention clinical trial is performed to assess the safety and suitability of an infant formula manufactured from extensively hydrolysed protein by showing normal growth of healthy term infants during the first 120 days of life with an optional follow up until 180 days of life.

NCT ID: NCT04400396 Enrolling by invitation - Prematurity Clinical Trials

Effect of Target Fortified Human Milk on the Growth Quality of Very Preterm Infants (TargetFort)

TargetFort
Start date: February 1, 2020
Phase:
Study type: Observational

It is reported that the standard method for fortification of human milk (HM) overestimates the energy and protein densities of HM (Macedo MHNP 2018), thus originating infant undernutrition (Macedo AJP 2018). The target fortification, based on analysis of HM composition, is considered the gold-standard method (Rochow 2015, McLeod 2016). This observational mixed cohort study aims to assess if very preterm infants fed HM with target fortification have greater growth during hospital stay and better body composition at term post-menstrual age (PMA), than those fed HM with standard fortification.

NCT ID: NCT04392063 Completed - Cerebral Palsy Clinical Trials

Melatonin for Cerebral Palsy Children's Sleep and Health

Start date: June 2016
Phase: N/A
Study type: Interventional

The present study was prospective uncontrolled, single-armed and un-blinded study. Held in the Pediatric neurology clinic, Children's hospital l, Faculty of Medicine, Ain Shams University from June 2016 to June 2018 of 24 months timeframe. All cerebral palsy (CP) patients following up in Pediatric neurology clinic aged between 2 and 12 years. Melatonin given for 3 months. Anthropmetric measures, gastroeintestinal symptoms, Children's sleep habits questionnaire (CSHQ) Arabic version, polysomnography, Chalfont epilepsy severity score, and EEG were done at enrollment and after the 3-months.