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Sponsored by: |
Children's Hospital, San Diego |
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Information provided by: | Children's Hospital, San Diego |
ClinicalTrials.gov Identifier: | NCT00490607 |
The purpose of this study is to investigate the pathogenesis of hemangiomas of infancy as they relate to normal pregnancies and those pregnancies complicated by placenta abnormalities. Women of all gestational ages will be enrolled in the study. Maternal serum, placental, and cord blood samples will be obtained for each subject. A medical history will be obtained for each subject. Post-delivery a member of the study team will perform a cutaneous exam of the infant to establish what birthmarks are present at birth. Mother will receive four phone call follow ups to determine if the infant has had any skin changes. If yes, mother will be asked to bring the child in for evaluation. If a hemangioma is diagnosed, a blood draw will be performed.
Condition |
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Hemangioma |
Study Type: | Observational |
Study Design: | Longitudinal, Defined Population, Prospective Study |
Genders Eligible for Study: | Female |
Inclusion Criteria:
United States, California | |
Sharp Mary Birch Hospital for Women | Recruiting |
San Diego, California, United States | |
Contact: Andrea M Munden, BS 858-576-1700 ext 5210 amunden@rchsd.org |
Principal Investigator: | Sheila F Friedlander, MA | Children's Hospital, San Diego |
Study ID Numbers: | Hemangioma Study |
Study First Received: | June 21, 2007 |
Last Updated: | June 21, 2007 |
ClinicalTrials.gov Identifier: | NCT00490607 |
Health Authority: | United States: Institutional Review Board |
Hemagiomas of infancy |
Hemangioma, Capillary Hemangioma Congenital Abnormalities |
Neoplasms Neoplasms by Histologic Type Neoplasms, Vascular Tissue |