Hemangioma Associated With High Rates of Morbidity
NCT00394888 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 433
Last updated 2013-09-20
Summary
We are conducting a study on the possible presence of PHACES in children with large facial hemangiomas and lumbosacral hemangiomas of infancy (hemangioma in the lower back) . With this study we hope to better understand the risk of this syndrome and to develop guidelines for its evaluation and management.
Conditions
- Hemangioma
Interventions
- DEVICE
-
MRI
MRI of the spine.
- DEVICE
-
MRI of head and neck
MRI of head and C-spine
- OTHER
-
Dermatological Examination
Complete dermatological examination to identify and characterize nature of dermatological anomalies
- OTHER
-
Cardiac examination
Complete cardiac examination
- DEVICE
-
Abdominal ultrasound
Abdominal ultrasound to detect hepatic hemangiomas
Sponsors & Collaborators
-
University of California, San Francisco
collaborator OTHER - collaborator OTHER
-
Baylor College of Medicine
collaborator OTHER -
St. Justine's Hospital
collaborator OTHER -
State University of New York - Downstate Medical Center
collaborator OTHER -
Children's Mercy Hospital Kansas City
collaborator OTHER -
Children's Hospital Medical Center, Cincinnati
collaborator OTHER -
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
collaborator OTHER -
Medical College of Wisconsin
lead OTHER
Principal Investigators
-
Beth Drolet, MD · Medical College of Wisconsin
-
Maria Garzon, MD · Columbia University
-
Denise Metry, MD · Baylor College of Medicine
-
Ilona Frieden, MD · University of California, San Francisco
-
Julie Powell, MD · Hopital Sainte-Justine
-
Anne Lucky, MD · Children's Hospital of Cincinnati
-
Sharon Glick, MD · State University of New York - Downstate Medical Center
-
Eulalia Baselga, MD · Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
-
Anita Haggstrom, M.D. · Indiana University
-
Anthony Mancini, MD · Northwestern University
-
Kimberly Horii, MD · Children's Mercy Hospital Kansas City
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- SCREENING
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-11-30
- Primary Completion
- 2009-11-30
- Completion
- 2010-01-31
Countries
- United States
Study Locations
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