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Infant, Newborn, Diseases clinical trials

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NCT ID: NCT02447159 Completed - HIV Infections Clinical Trials

Evaluation of Conditional Cash Transfers to Increase Retention in PMTCT Services in Akwa Ibom State, Nigeria

Start date: August 2015
Phase: N/A
Study type: Interventional

A randomized controlled trial will be conducted to assess the effectiveness of conditional cash transfers (CCTs) at increasing retention in prevention of mother-to-child transmission (PMTCT) services specifically, in relation to pickup of ARV drugs for infected mothers, delivery in the hospital setting, and receipt of drugs for exposed infants. Administrative data will be extracted from the All Babies are Equal program and hospital records. At 8-10 weeks after delivery, an endline survey will also be conducted with each participant to provide a deeper understanding of the impact of the CCTs and to assess the reasons for retention in PMTCT services.

NCT ID: NCT02434380 Completed - Clinical trials for Pregnancy Complications

Effect of Vitamin D Replacement on Maternal and Neonatal Outcomes

Start date: July 2015
Phase: Phase 3
Study type: Interventional

The optimal vitamin D replacement dose during pregnancy remains undefined. Therefore, the aim of this study is to test the hypothesis that a daily equivalent dose of vitamin D of 3,000 IU/day is needed for Middle Eastern women, to optimize maternal vitamin D level and neonatal musculoskeletal parameters, specifically knee-heel length at birth and bone mineral content at one month of age.

NCT ID: NCT02410486 Completed - Clinical trials for Infant, Newborn, Diseases

Early-Onset Sepsis an NICHD/CDC Surveillance Study

EOSII
Start date: April 2015
Phase:
Study type: Observational

This prospective surveillance study will be conducted over a 2 year period to determine current rates of Early-Onset Sepsis (EOS)/ Early-Onset Meningitis (EOM), associated pathogens, antimicrobial resistance, signs and symptoms and infant outcomes.

NCT ID: NCT02375828 Completed - Clinical trials for Neonatal Diabetes Secondary to Mutation in the Potassium Channel

Glibentek in Patients With Neonatal Diabetes Secondary to Mutations in K+-ATP Channels

NEOGLI
Start date: March 20, 2015
Phase: Phase 3
Study type: Interventional

The understanding of the molecular mechanisms of neonatal diabetes has deeply changed the therapy of patients carrying mutations in the K-ATP channel. Indeed, those patients are not treated anymore by insulin injections but by glibenclamide an oral anti-diabetic drug widely used in type 2 diabetes. Anyway, its galenic form (pills of 5 mg) is not suitable for children and difficult to administrate to infants or young children. The purpose of this study is to determine if a new galenic form of this durg is more suitable and as efficient as pills in children with neonatal diabetes.

NCT ID: NCT02068807 Completed - Clinical trials for Infant, Newborn, Diseases

Evaluation of Antioxidant Activity of Oral Lutein in Preterm and Term Newborn

Start date: January 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The balance of the redox state is important for normal embryonic and fetal development . During the perinatal period, a variety of conditions are responsible for an excessive production of free radicals. The following oxidative stress is exacerbated by a lack of antioxidant substances that have not yet matured. At the moment there are no therapeutic strategies with single or combined antioxidants that have been shown to be clinically effective. Breastfeeding is important for the contribution of the antioxidant defenses of the newborn and the nutritional status of the mother plays a key role because it influences the nutritional status of the newborn. Lutein is a carotenoid that is not produced by the body , but taken with food or supplements. The molecule carries out different activities : antioxidant, anti-inflammatory, anticancer , neuroprotective. Its main activity of inhibition of peroxidation of membrane lipids is peculiarly important for the photoreceptors and neurons whose membranes are rich with polyunsaturated fatty acids. Current evidence on its role as an antioxidant indicate that supplementation with lutein may play a significant role in the prevention of free radical disease in the newborn

NCT ID: NCT01954056 Completed - Clinical trials for Infant, Newborn, Diseases

Hydrocortisone for Term Hypotension

Start date: June 19, 2014
Phase: Phase 3
Study type: Interventional

This trial will evaluate the effects of a 7-day course of hydrocortisone therapy on short-term morbidity, cardiovascular function, long-term neurodevelopment, and mortality in critically ill, term and late preterm infants diagnosed with cardiovascular insufficiency as defined by a need for inotrope therapy in the first 72 hours of age.

NCT ID: NCT01899651 Completed - Clinical trials for Intraventricular Brain Hemorrhage

Detection and Quantification of Neonatal Intraventricular Hemorrhage

DQNIH
Start date: May 2014
Phase: N/A
Study type: Observational

Dense array EEG and EIT (electrical impedence tomography) are new technologies that can add to information needed to diagnose neurological problems in infants - both preterm and term. The investigators propose a method to test these technologies in the preterm population to determine its safety and ease of use. The investigators will test on preterm infants of 30-34 weeks gestation, starting first with the older infants (32-34 weeks) then moving down to the smaller population (30-32 weeks). In both groups the investigators will start with a short time period and gradually extend the time as safety is established. All studies will be conducted at Shands Teaching Hospital at the University of Florida.

NCT ID: NCT01702805 Active, not recruiting - Anemia Clinical Trials

Transfusion of Prematures Trial

TOP
Start date: December 2012
Phase: Phase 3
Study type: Interventional

The objective of the TOP trial is to determine whether higher hemoglobin thresholds for transfusing ELBW infants resulting in higher hemoglobin levels lead to improvement in the primary outcome of survival and rates of neurodevelopmental impairment (NDI) at 22-26 months of age, using standardized assessments by Bayley.

NCT ID: NCT01621373 Completed - Clinical trials for Adverse Reaction to Drug

Exploratory Propofol Dose Finding Study In Neonates

NEOPROP
Start date: August 2012
Phase: Phase 2
Study type: Interventional

The aim of the study is to explore the optimal propofol dose in neonates receiving a single intravenous propofol bolus for endotracheal intubation during (semi-)elective INSURE (intubation-surfactant-extubation) procedure (preterm neonates) and (semi-)elective non-INSURE procedures (term-preterm neonates).

NCT ID: NCT01514253 Not yet recruiting - Clinical trials for Infant, Newborn, Diseases

Reduced Infant Response to a Routine Care Procedure After Glucose 25% Analgesia in Comparison to Materna RTF Stage 1

glucose
Start date: February 2012
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 in comparison to Materna RTF Stage 1 for procedural pain on infant pain responses during a subsequent care giving procedure.