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Anemia, Neonatal clinical trials

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NCT ID: NCT00731588 Completed - Neonatal Anemia Clinical Trials

Red Blood Cell (RBC) Survival Following Transfusion in Infants

Start date: June 2008
Phase: Phase 2
Study type: Interventional

OUR OVERALL HYPOTHESIS is that post-transfusion survival of allogeneic and autologous RBCs can be accurately quantified in anemic human infants using biotin-labeled RBCs combined with mathematical modeling that adjusts for confounding factors commonly encountered in neonates. These confounding factors include 1) dilution of labeled RBC as a result of growth stimulated erythropoiesis, anemia stimulated erythropoiesis, and blood transfusion; 2) loss of labeled RBC due to laboratory phlebotomy; and 3) variable RBC life spans resulting from RBCs having been produced at different developmental periods and under varying rates of erythropoiesis. In contrast to infants, adjustment for these factors is not necessary in healthy adults under conditions of steady state erythropoiesis. Instead in adults, RBC survival is typified by a linear decline in concentration of labeled RBCs over time. When this line is extrapolated to zero concentration, the intercept with the time axis represents the mean potential lifespan (MPL) of RBCs. (<7 d) and stored (>21 d) allogeneic adult RBCs transfused in the same infant.

NCT ID: NCT00458068 Completed - Iron Deficiency Clinical Trials

Early Versus Late Enteral Iron in Infants Less Than 1301 Grams

Start date: June 1996
Phase: N/A
Study type: Interventional

Background: Preterm infants are at risk of iron deficiency. The smaller the infants are at birth, the smaller the iron stores at birth and the higher the risk of iron deficiency. Hypothesis: Preterm infants with a birth weight of less than 1301g require iron supplementation earlier than previously recommended. Methods: Prospective randomized controlled clinical trial (1996-1999). Results: Early iron supplementation may reduce the incidence of iron deficiency and the need for late blood transfusions.

NCT ID: NCT00457990 Completed - Iron Deficiency Clinical Trials

Neurodevelopment After Early Iron Supplementation

Start date: April 2002
Phase: N/A
Study type: Interventional

Background: Iron deficiency in early childhood may impair neurodevelopment. Aim: To examine whether early iron supplementation improved neurodevelopment in preterm infants. Method: Children who participated in a clinical trial of iron supplementation were invited for a neurodevelopmental follow-up examination at the time of school entry.

NCT ID: NCT00182390 Completed - Clinical trials for Anemia of Prematurity

Premature Infants in Need of Transfusion (PINT)

Start date: February 2001
Phase: Phase 3
Study type: Interventional

Hypothesis: That a high hemoglobin threshold for transfusion in extremely low birth weight (ELBW) infants is associated with a lower rate of survival without severe morbidity (defined as one or more of retinopathy of prematurity, bronchopulmonary dysplasia, or periventricular leukomalacia/ventriculomegaly). Primary Objective: To determine whether either a liberal or more restrictive threshold of hemoglobin level for red cell transfusion in ELBW infants is safer, by randomizing to either a high transfusion hemoglobin threshold or a low transfusion hemoglobin threshold. Follow-up at a corrected age of 18 months represents a conventional age at which to first assess neurodevelopmental outcomes, and to predict long-term outcomes.

NCT ID: NCT00167388 Completed - Clinical trials for Anemia of Prematurity

The Effect of Blood Transfusion on Blood Flow to the Intestines of Premature Infants

Start date: September 2005
Phase: Phase 1
Study type: Interventional

The purpose of the study is to see if a blood transfusion changes how fast blood flows to the intestines of a premature baby. Blood flow is measured by an ultrasound test. The investigators also look to see if the blood flow to the intestines depends on whether the baby feeds or doesn't feed during the blood transfusion.