Clinical Trials Logo

Infant, Newborn clinical trials

View clinical trials related to Infant, Newborn.

Filter by:

NCT ID: NCT00011362 Completed - Clinical trials for Bronchopulmonary Dysplasia

Dexamethasone Therapy in VLBW Infants at Risk of CLD

Dexamethasone
Start date: September 1992
Phase: Phase 3
Study type: Interventional

Infants who are on breathing support are often treated with steroids (dexamethasone); however, the best timing of therapy is not known. This trial looked at the benefits and hazards of starting dexamethasone therapy at two weeks of age and four weeks of age in premature infants.

NCT ID: NCT00009620 Completed - Infant, Premature Clinical Trials

Antenatal Phenobarbital to Prevent Neonatal Intracranial Hemorrhage

Phenobarbital
Start date: February 1993
Phase: Phase 3
Study type: Interventional

This large randomized trial tested whether phenobarbital given to a pregnant woman about to deliver a premature infant would prevent brain injuries in their newborns. Women with 24 to 32 week fetuses who were in preterm labor and were expected to deliver within 24 hrs were randomized to phenobarbital or usual care. They were treated until they deliver or the fetus reaches 33 wks gestation. Babies were followed until discharge and evaluated at 18-22 mos corrected age for neurodevelopmental outcome.

NCT ID: NCT00005775 Completed - Sepsis Clinical Trials

Glutamine Supplementation to Prevent Death or Infection in Extremely Premature Infants

Glutamine
Start date: July 1999
Phase: Phase 3
Study type: Interventional

This large multicenter double-masked clinical trial tested whether supplementation of standard neonatal parenteral nutrition with glutamine would reduce the risk of death or late-onset sepsis in extremely-low-birth-weight (ELBW, less than or equal to 1000 gm) infants. Neonates with birth weights of 401-1000gm were randomized to standard TrophAmine or TrophAmine supplemented with glutamine before 72 hours and continued until the infants are tolerating full enteral feedings.

NCT ID: NCT00005772 Completed - Infant, Newborn Clinical Trials

Whole-Body Cooling for Birth Asphyxia in Term Infants

Start date: October 1999
Phase: Phase 3
Study type: Interventional

This large multicenter trial tested whether cerebral cooling initiated within 6 hours of birth and continued for 72 hours would reduce the risk of death and moderate to severe neurodevelopmental injury at 18-22 months corrected age. Infants at least 36 weeks gestation with an abnormal blood gas within 1 hour of birth, or a history of an acute perinatal event and a 10-min Apgar score <5, or continued need for ventilation were screened. Following a neurological exam, those with moderate to severe encephalopathy were randomized to a 72-hour period of total body cooling (cooling blanket, followed by slow re-warming). The study was conducted in two phases: Phase I (20 infants) were examined for the safety of an esophageal temperature of 34-35 C; Phase II (main trial, 200 infants) were evaluated for the safety and efficacy of an esophageal temperature of 33-34 C. Cardio-respiratory, electroencephalograms (EEGs), renal, metabolic, and hematologic status, and esophageal and abdominal skin temperature were monitored during the 72 hours of intervention. Surviving children were given neurodevelopmental examinations at 18-22 months corrected age and again at school age (6-7 years of age).