Erythropoietin for Infants With Brain Injuries Due to Oxygen Deprivation at Birth
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|ClinicalTrials.gov Identifier: NCT00491413|
Recruitment Status : Unknown
Verified August 2003 by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).
Recruitment status was: Not yet recruiting
First Posted : June 26, 2007
Last Update Posted : June 26, 2007
|Condition or disease||Intervention/treatment||Phase|
|Asphyxia||Drug: epoetin||Phase 1|
Damage to the central nervous system as a result of oxygen deprivation at birth is a major cause of life-long mental and developmental handicaps. When there is not enough oxygen in the blood (hypoxemia) the brain is deprived of oxygen. Some brain cells respond by producing Epo. Epo then binds to oxygen-deprived brain cells. This binding triggers chemical reactions within the brain cell that prevent cell death. Epo also reduces inflammation around the brain cells and acts as an antioxidant. In animal studies, recombinant Epo (rEpo) administration, even up to six hours after oxygen deprivation, reduced subsequent brain injury by 50% to 70%.
Epo has been used by neonatologists to stimulate erythropoiesis (red blood cell production) and reduce the incidence of blood transfusions. Doses of rEpo required for protection of brain cells are considerably higher than those traditionally used by neonatologists.
This study will evaluate the pharmacokinetics, biologic effect, and safety of high dose Epo in neonates with brain injury due to hypoxemia.
Within six hours of birth, each eligible infant will receive one dose of rEpo intravenously. Any infants who require a lumbar puncture during the first week of life will have levels of natural Epo and rEpo in their spinal fluid measured. Blood tests will be used to measure the antioxidant effect of Epo and the impact on red blood cell production. Neurodevelopmental outcome will be measured at 6 and 12 months of age.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||15 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||High Dose Erythropoietin for Neonates With Asphyxia|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00491413
|United States, Florida|
|All Children's Hospital||Not yet recruiting|
|St. Petersburg, Florida, United States, 33701|
|Contact: Robert D. Christensen, MD 727-502-8168 email@example.com|
|Contact: Stacey M. Levitt, MD 727-553-1570 firstname.lastname@example.org|
|Principal Investigator:||Robert D. Christensen, MD||University of South Florida|