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Birth Weight clinical trials

View clinical trials related to Birth Weight.

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NCT ID: NCT00873847 Completed - Infant, Premature Clinical Trials

Cerebral Function Monitoring in Premature Infants

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

This observational study tests the feasibility of enrolling subjects and obtaining an amplitude-integrated electroencephalogram (aEEG) within the first 72 hours of life, a second aEEG recording between 72-168 hours of life, and weekly thereafter up to 36 weeks post-menstrual age. It will enroll 85-100 infants between 401-1,000 grams birth weight OR between 23 0/7 and 28 6/7 weeks gestational age born at the 7 participating NICHD Neonatal Research Network sites.

NCT ID: NCT00860470 Completed - Preterm Birth Clinical Trials

Antenatal Micronutrient Supplementation and Infant Survival

JiVitA-3
Start date: January 2008
Phase: Phase 3
Study type: Interventional

The purpose of this community-based randomized trial is to examine whether a daily antenatal and postnatal multiple micronutrient supplement given to women will enhance newborn and infant survival and health and other birth outcomes in a rural setting in northwestern Bangladesh.

NCT ID: NCT00850902 Not yet recruiting - Clinical trials for Extremely Low Birth Weight

Humidity Strategy to Decrease Morbidity and Mortality in Extremely Low Birth Weight Infants

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to apply a different incubator humidity strategy at birth to decrease morbidity and mortality in extremely low birth (1000 g or less) infants.

NCT ID: NCT00840983 Completed - Clinical trials for Bronchopulmonary Dysplasia

Effects of Delayed Cord Clamping in Very Low Birth Weight Infants

Start date: August 2003
Phase: Phase 1
Study type: Interventional

The purpose of this study was to see if a brief delay in cord clamping for 30 to 45 seconds would result in higher hematocrit levels, fewer transfusions, healthier lungs, and better motor function at 40 wks and 7 months of age.

NCT ID: NCT00813657 Completed - Clinical trials for Gestational Diabetes Mellitus

Resistance Exercise Training During Pregnancy: a Randomized Controlled Trial

Start date: January 2000
Phase: Phase 4
Study type: Interventional

The investigators investigated the effects of a supervised maternal exercise training program (performed during the 2nd and 3rd trimesters of pregnancy) on maternal-newborn unit health outcomes in a group of previously sedentary healthy women. A matched control group was assessed over the same time period. Given the fact that most studies in the field have used aerobic exercises, here the investigators largely focused on very light resistance, toning exercises.

NCT ID: NCT00799721 Recruiting - Clinical trials for Infant, Very Low Birth Weight

Urine VEGF Levels in Very Low Birth Weight (VLBW) Infants

Start date: August 2008
Phase: N/A
Study type: Observational

VLBW infants are at risk of developing retinopathy of prematurity (ROP). In the first phase of ROP there is a down-regulation of retinal VEGF-expression because of postnatal relative hyperoxia, followed by an upregulation of VEGF mediated through retinal hypoxia, which leads to pathologic vessel formation. VEGF acts through binding to the specific receptor FLT-1, the soluble form sFLT-1 is a specific antagonist of VEGF action. Erythropoietin, given to VLBW infants to prevent anemia, may stimulate VEGF-production in neuronal cells. Currently, there are no data published about VEGF urine-levels in VLBW infants and it is not known, if urine VEGF-levels may serve as a non-invasive marker of ROP-risk. Further shall be investigated, if erythropoietin-therapy increases urine VEGF-levels and if there is a correlation with ROP-development.

NCT ID: NCT00760942 Completed - Clinical trials for Infant, Very Low Birth Weight

Liquid Preterm Formula Versus Powdered Human Milk Fortifier in VLBW Infants

Start date: October 2008
Phase: N/A
Study type: Interventional

This study aims to compare the short-term effects on growth and feeding tolerance of a liquid high calorie formula added to human milk versus powdered human milk fortifier in small preterm infants.

NCT ID: NCT00747240 Completed - Clinical trials for Low Birth Weight Infant

Platelet-activating Factor Acetylhydrolase (Paf-ah) Gene Expression

Start date: February 2002
Phase: N/A
Study type: Observational

This is a prospective observational study to determine whether there is an association between the presence of platelet-activating factor acetylhydrolase (PAF-AH) gene polymorphisms and the development of chronic lung disease in very low birth wight infants. Infants < 1500 grams at birth who require mechanical ventilation will be enrolled in the first 5 days of life after obtaining informed consent. A total of 1 ml of blood will be drawn and utilized for isolation of DNA for genotyping and for measurement of PAF-AH activity in serum.

NCT ID: NCT00715000 Completed - Enteral Nutrition Clinical Trials

Oral Versus Intravenous Rehydration for Prevention of Dehydration in Premature Babies, During the First Days of Life.

SROPREMA
Start date: July 2008
Phase: Phase 4
Study type: Interventional

This prospective randomised study comparing administration of a hypo-osmolar oral hydration solution with the classical hydration via IV (intravenous) infusion in premature infants of more than 32 weeks GA (gestational age) aims to determine whether administration of a hypo-osmolar oral hydration solution is as efficient as intravenous infusion.

NCT ID: NCT00710112 Recruiting - Clinical trials for Chronic Lung Disease

Genetic Variants and Susceptibility to Diseases of Prematurity in Very Low Birth-Weight Infants

CLD
Start date: June 2006
Phase:
Study type: Observational

The purpose of this study is to determine if sequence variations in genes involved in the development and function of vulnerable organs increases susceptibility to chronic lung disease (CLD) and other diseases affecting premature infants, such as necrotizing enterocolitis (NEC), sepsis, patent ductus arteriosus (PDA) and intraventricular hemorrhage (IVH). The study will also determine whether measurement of certain biomarkers in serum will identify infants who will develop these complications of prematurity. Previous studies from this institution and others have identified genetic variants in some genes, such as toll like receptor genes are associated with higher risk of CLD or NEC. The interaction of these variants with other gene variants that can influence the risk of these diseases remains unclear.