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| Sponsor: | Johns Hopkins University |
|---|---|
| Collaborator: |
Hugo W. Moser Research Institute at Kennedy Krieger, Inc. |
| Information provided by: | Johns Hopkins University |
| ClinicalTrials.gov Identifier: | NCT00131859 |
Purpose
The researchers' objective is to use diffusion-tensor imaging (DTI) to evaluate infants diagnosed with cerebral white matter injury during the neonatal period and identify antenatal risk factors, electronic fetal heart rate monitoring abnormalities, and umbilical arterial gas results that are associated with cerebral white matter injury. The researchers' hypothesis is that this new imaging technique will help us better understand how these devastating injuries occur.
| Condition | Intervention |
|---|---|
|
Brain Injury, Fetus and Neonate |
Procedure: Diffusion-tensor imaging |
| Study Type: | Observational |
| Study Design: | Case Control, Prospective |
| Official Title: | Diffusion-Tensor Magnetic Resonance Imaging and the Evaluation of Perinatal Brain Injury |
| Enrollment: | 5 |
| Study Start Date: | October 2004 |
| Study Completion Date: | December 2008 |
| Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
Maternal and neonatal data will be collected as well as the umbilical arterial gas results and the electronic fetal heart rate tracing of the labor. Infants will have a head ultrasound at 24-72 hours, 10-14 days, and at 4-6 weeks to look for cerebral white matter injury, as standard of care. All infants with a birth weight < 1500 grams will be offered DTI, and infants > 1500 grams with white matter injury diagnosed by ultrasound will be imaged as well as the subsequent delivery born within 7 days of that gestational age without brain injury. All infants will have the DTI brain scan at 12-18 months of age corrected for the degree of prematurity, and will also have a formal neurological assessment at that time.
Eligibility| Ages Eligible for Study: | 23 Weeks to 18 Months |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Neonates < 1500 grams, with suspected brain injury, and with severe metabolic acidosis
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Maryland | |
| Johns Hopkins Hospital | |
| Baltimore, Maryland, United States, 21287 | |
| Johns Hopkins Hospital | |
| Baltimore, Maryland, United States, 21287-1228 | |
| Principal Investigator: | Ernest M Graham, M.D. | Johns Hopkins Univ; Dept. of Gyn-Ob |
More Information
| Responsible Party: | Johns Hopkins University School of Medicine ( Ernie Graham, M.D. ) |
| Study ID Numbers: | 04-08-31-01 |
| Study First Received: | August 18, 2005 |
| Last Updated: | August 12, 2009 |
| ClinicalTrials.gov Identifier: | NCT00131859 History of Changes |
| Health Authority: | United States: Institutional Review Board |
|
Perinatal brain injury Diffusion-tensor imaging |
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Craniocerebral Trauma Nervous System Diseases Wounds and Injuries Disorders of Environmental Origin |
Central Nervous System Diseases Trauma, Nervous System Brain Diseases Brain Injuries |