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Birth Weight clinical trials

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NCT ID: NCT01430832 Terminated - Clinical trials for Post Traumatic Stress Disorder

Developmental Outcomes of Extreme Prematurity, 5-15 Years Postpartum

Start date: September 1, 2011
Phase:
Study type: Observational

The purpose of this study is to assess the emotional well being of mothers to preterm infants with ELBW 5-15 years after the birth. Post-traumatic symptoms and parental stress levels will be taken into consideration. In addition, the correlation between the infant's development and the mother's emotional state will be analyzed.

NCT ID: NCT01430728 Recruiting - Clinical trials for Infant, Very Low Birth Weight

Cerebral Tissue Oxygenation in Very Low Birthweight Infants in the First 3 Days of Life

Start date: April 2011
Phase: N/A
Study type: Observational

The purpose of this study is to examine the range of cerebral tissue oxygen saturation in healthy and sick very low birthweight infants during the first 72 hours of life.

NCT ID: NCT01424553 Completed - Clinical trials for Bronchopulmonary Dysplasia

Respiratory Outcome at Adolescence of Very Low Birthweight Infants

EPIPAGEADO
Start date: October 2011
Phase: N/A
Study type: Interventional

EPIPAGEADO is an observational study. Respiratory symptoms and lung function will be evaluated in very low birth weight and term infants, born in 1997 and included in the French EPIPAGE cohort.

NCT ID: NCT01420029 Completed - Clinical trials for Low Birth Weight Neonates

Hospital-Based Phthalate Exposure in Very Low Birth Weight Neonates

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

In this observational pilot project, the investigators plan to document duration and sources of exposure to plasticizers in infants born at birth weights less than 1500 grams. The investigators will examine the association between exposure to plasticizers and outcomes such as performance on a neurological screening tool, extrauterine growth, and thyroid function.

NCT ID: NCT01419873 Completed - Hyperglycaemia Clinical Trials

Study of a Model-based Approach to Blood Glucose Control in Very-low-birthweight Neonates

Start date: August 2008
Phase: Phase 4
Study type: Interventional

Very low birthweight neonates commonly develop high blood sugar levels. There is an association between high blood sugar levels and poorer short term outcomes but it is not known whether the high sugar level itself actually causes the problems. There are a range of ways to manage high sugar levels but there are no consensus guidelines to follow. One option is to manage the high sugar levels with an infusion of insulin. Studies looking at insulin infusions have often used fixed protocols to guide the amount of insulin to be given and are often complicated by hypoglycaemia. This study investigated whether using a model-based approach to individualise insulin administration to neonates with high sugar levels would provide a safe and effective management option for controlling blood sugar levels and avoid the complication of low blood sugar levels.

NCT ID: NCT01411748 Recruiting - Clinical trials for Anticandidal Property of Saccharomyces Boulardii on Very Low Birth Weight Infants

Comparison of Saccharomyces Boulardii and Nystatin Prophylaxis on Candida Colonization and Infection in Very Low Birth Weight Infants

Start date: July 2011
Phase: Phase 4
Study type: Interventional

Probiotics are favorable microorganisms that regulate the flora of the gastrointestinal system and stimulate the immune system. Saccharomyces boulardii was shown to reduce candida colonization. The objective of this study is to evaluate the efficacy of prophylactic S boulardii in reducing the candida colonization and infection in very low birth weight infants.

NCT ID: NCT01400737 Recruiting - Clinical trials for Oral Ibuprofen Prophylaxis in Very Low Birth Weight Infants

Oral Ibuprofen Prophylaxis for Patent Ductus Arterioses in Very Extremely Low Birth Weight Infants

OIP
Start date: July 2011
Phase: N/A
Study type: Interventional

Patent ductus arterioses (PDA) is a major morbidity in preterm infants, especially in extremely premature infants less than 28 weeks. The clinical signs and symptoms of PDA in preterm infants are non specific and insensitive for making an early diagnosis of significant ductal shunting. Functional echocardiography is emerging as a new valuable bedside tool for early diagnosis of hemodynamically significant ductus, even though there are no universally accepted criteria for grading the hemodynamic significance. Echocardiography has also been used for early targeted treatment of ductus arterioses, though the long term benefits of such strategy are debatable. The biomarkers like BNP and N- terminal pro-BNP are currently under research as diagnostic marker of PDA. The primary mode of treatment for PDA is pharmacological closure using cyclo-oxygenase inhibitors with closure rate of 70-80%. Oral ibuprofen is emerging as a better alternative especially in Indian scenario where parenteral preparations of indomethacin are unavailable and side effects are comparatively lesser. Though pharmacological closure of PDA is an established treatment modality, there is still lack of evidence for long term benefits of such therapy as well as there is some evidence for the possible adverse effects like increased ROP and BPD rates, especially if treated prophylactically.The aim of this study is to investigate the effect of oral ibuprofen prophylaxis administrated on the first 24 hours of life and the following two days on hemodynamically significant patent ductus arterioses and its long term effects such as ROP and BPD.

NCT ID: NCT01393496 Completed - Clinical trials for Anemia of Prematurity

Effects of Transfusion Thresholds on Neurocognitive Outcome of Extremely Low Birth Weight Infants

ETTNO
Start date: July 2011
Phase: Phase 4
Study type: Interventional

To compare the effect of restrictive versus liberal red blood cell transfusion thresholds on long-term neurodevelopmental outcome in extremely low birth weight infants.

NCT ID: NCT01390051 Completed - Clinical trials for Fetal Growth Retardation

Can Low Molecular Weight Heparin During Pregnancy With Intrauterine Growth Restriction Increase Birth Weight?

IUGR
Start date: July 2011
Phase: Phase 4
Study type: Interventional

The purpose of the study is to investigate if treatment with an anticoagulant drug increases birth weight in pregnancies complicated by fetal growth restriction.

NCT ID: NCT01385254 Completed - Clinical trials for Very Low Birthweight

Mother Sibling Interactions Following Very Low Birth Weight (VLBW) Infant Homecoming

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

The proposed study will explore longitudinally the impact of a very low birthweight (VLBW) infant on mother-sibling interactions and sibling adjustment. The study will also include a comparison group of fullterm infants to determine which sibling adjustment problems are typical of having a new baby in the home and which are associated with the unique stress of having a VLBW infant. This study will be the initial step in identifying factors affecting the adjustment of siblings of VLBW infants.