- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00490607
A Prospective Study Comparing the Incidence of Infantile Hemangiomas Following Normal Pregnancies Versus Pregnancies Complicated by Placental Abnormalities
June 21, 2007 updated by: Rady Children's Hospital, San Diego
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.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
San Diego, California, United States
- Recruiting
- Sharp Mary Birch Hospital for Women
-
Contact:
- Andrea M Munden, BS
- Phone Number: 5210 858-576-1700
- Email: amunden@rchsd.org
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- pregnant women delivering at Sharp Mary Birch Hospital for Women in San Diego, CA
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Sheila F Friedlander, MA, Rady Children's Hospital, San Diego
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
June 21, 2007
First Submitted That Met QC Criteria
June 21, 2007
First Posted (Estimate)
June 25, 2007
Study Record Updates
Last Update Posted (Estimate)
June 25, 2007
Last Update Submitted That Met QC Criteria
June 21, 2007
Last Verified
June 1, 2007
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Hemangioma Study
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Hemangioma
-
Cairo UniversityCompleted
-
Zhujiang HospitalUnknownInfantile Hemangioma | Capillary Hemangioma | Capillary Hemangiomas | Hemangioma, Capillary Infantile | Strawberry HemangiomaChina
-
Tehran University of Medical SciencesCompletedHemangioma LiverIran, Islamic Republic of
-
Vitreous -Retina- Macula Consultants of New YorkRegeneron PharmaceuticalsNo longer available
-
Second Affiliated Hospital, School of Medicine,...Terminated
-
Southwest Hospital, ChinaCompleted
-
Joyce TengStanford UniversityNot yet recruiting
-
Nancy BaumanTerminatedHemangioma of InfancyUnited States
-
Assiut UniversityUnknownManagement of Intracranial Cavernous Hemangioma