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Infants clinical trials

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NCT ID: NCT06353841 Recruiting - Constipation Clinical Trials

Effect of Therapeutic Touch on Functional Constipation in Infants and Young Children

Start date: May 3, 2023
Phase: N/A
Study type: Interventional

The aim of the study is to determine the effect of therapeutic touch on functional constipation in infants and young children.

NCT ID: NCT06318858 Recruiting - Anemia Clinical Trials

Daily and Weekly Iron Supplementation in Infants

Start date: March 15, 2023
Phase: N/A
Study type: Interventional

This study aims to compare the efficacy of daily iron supplementation and weekly iron supplementation in infants aged 6-12 months on the prevalence of anemia, hemoglobin level, and serum ferritin levels. Infants will be enrolled at 6 months and will be randomly assigned to receive either daily or weekly iron supplementation for the first 3 months and will be followed by weekly iron supplementation for another 3 months.

NCT ID: NCT05940688 Recruiting - Pregnancy Clinical Trials

Providing an Optimized and emPowered Pregnancy for You (PᵌOPPY) Feasibility Study

P?OPPY
Start date: July 17, 2023
Phase: N/A
Study type: Interventional

The P3OPPY Project is one of five projects within the American Heart Association P3 EQUATE Network. The overarching goal of the P3 EQUATE American Heart Association Health Equity Research Network (HERN) is to promote equity in Maternal and Infant Health outcomes by identifying innovative and cost-effective strategies to enhance access to quality health information, care, and experiences during pregnancy, postnatal and postpartum/preconception periods, particularly for Black and under-served populations. Collectively, the investigators will collaborate with pregnant and postpartum individuals and their families, hospitals, and communities to discover ways to reduce racism and social problems that contribute to poor health outcomes.

NCT ID: NCT05705258 Recruiting - Clinical trials for Retinopathy of Prematurity

A Study to Collect Data on the Use of Eylea in Babies Born Too Early Who Have a Condition of the Eye Where Blood Vessels Grow Abnormally in the Retina (Retinopathy of Prematurity)

Start date: March 27, 2023
Phase:
Study type: Observational

This is an observational study to collect data from Japanese babies with retinopathy of prematurity (ROP) who will be treated with Eylea. In observational studies, only observations are made without specified advice or interventions. ROP is a condition that affects the eye and occurs only in babies who are born too early. Most cases of ROP are mild and get better without treatment, but more serious cases need to be treated in time. ROP happens when the blood vessels in the "retina" grow abnormally. The retina is the layer of tissue at the back of the eye that picks up light and sends messages to the brain. In babies with ROP, these abnormal blood vessels can leak. This causes damage to the retina and can sometimes move it out of place causing medical problems such as blindness. Eylea is received as an injection into the eye. It works by blocking a certain protein (VEGF) that can cause blood vessels in the retina to grow abnormally. Eylea is already available in Japan and is approved for doctors to prescribe to babies with ROP. The participants in this study are Japanese babies with ROP that their doctors decided to treat with Eylea before the start of this study. Babies with ROP that were already prescribed Eylea by their doctors may also be included. The main purpose of this study is to collect more data on how safe the treatment with Eylea is in babies with ROP under a real-world setting. Another purpose of this study is to collect more data on how well Eylea works in these participants. To see how safe Eylea is, the study doctors will collect all medical problems that the participants treated with Eylea have. These medical problems are called adverse events. Doctors keep track of all the adverse events that happen, even if they do not think that they might be related to the treatment. To see how well Eylea works, the study doctors will check the number of participants: - with no active ROP after starting treatment - where ROP came back up to 6 months after start of treatment In this study, the study doctor will: - collect past data of the participants from medical records - interview the participants - collect treatment-related data during routine visits. The study duration is 6 months with 3 planned visits. One visit will be at start of treatment, one at one month and one at 6 months after start of treatment. All data required for this study will be collected during routine visits. Besides this data collection, no further tests or examinations are planned in this study.

NCT ID: NCT05492253 Recruiting - Clinical trials for Healthy Participants

First Complementary Foods and the Infant Gastrointestinal Microbiota

Start date: September 18, 2022
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: NCT01575184 Recruiting - Infants Clinical Trials

Effect of Shoulder Traction on Size and Relative Position of Internal Jugular Vein to Carotid Artery

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

Internal jugular vein (IJV) catheterization is frequently performed in infants undergoing major surgery. Although it has been suggested that head rotation increases the degree of overlapping between IJV and carotid artery (CA), IJV catheterization without head rotation is extremely difficult in infants. The aim of the present study is to evaluate whether the caudo-lateral traction of the ipsilateral arm can decrease the degree of overlapping between IJV and CA in infants during head rotation.