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Incidence of Ocular Antibodies in Patients With Sturge - Weber Syndrome (SWS)

This study is ongoing, but not recruiting participants.

Sponsors and Collaborators: University of California, Irvine
Mainz University
Information provided by: University of California, Irvine
ClinicalTrials.gov Identifier: NCT00610402
  Purpose

Sturge-Weber Syndrome (SWS) is a neurological disorder characterized at birth by seizures and a large port-wine stain birthmark on the forehead and upper eyelid of one side of the face. SWS is also accompanied by an increased pressure within the eye (glaucoma) which can develop very early in life.

Glaucoma represents a group of ocular disorders that are characterized by the loss of retinal ganglion cells and their axons, damage to the optic nerve, and gradual loss of visual field. Recently, several studies provided evidence that there is a potential role of the immune system in the pathogenesis of glaucoma.

These findings suggest that there might be changes in systemic humoral immunity possibly underlying the optic neuropathy in at least some glaucoma patients.


Condition
Sturge - Weber Syndrome (SWS)

Genetics Home Reference related topics:   hypohidrotic ectodermal dysplasia    Opitz G/BBB syndrome   

MedlinePlus related topics:   Glaucoma   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Case-Only, Prospective
Official Title:   Incidence of Ocular Antibodies in Patients With Sturge - Weber Syndrome (SWS)

Further study details as provided by University of California, Irvine:

Biospecimen Retention:   Samples Without DNA

Biospecimen Description:

blood sample tear drop sample


Estimated Enrollment:   100
Study Start Date:   July 2007
Estimated Study Completion Date:   July 2009
Estimated Primary Completion Date:   July 2009 (Final data collection date for primary outcome measure)

Detailed Description:

The ocular antibody profile in patients with SWS is unknown.The researchers want to study on blood and tear drop samples from patients with SWS to determine the incidence of ocular antibodies in patients with this syndrome.

  Eligibility
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample

Study Population

community sample


Criteria

Inclusion Criteria:

  • Male and female volunteers with SWS of all ages

Exclusion Criteria:

  • Volunteers without SWS
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00610402

Locations
United States, California
Beckman Laser Institute Medical clinic    
      Irvine, California, United States, 92612

Sponsors and Collaborators
University of California, Irvine
Mainz University

Investigators
Principal Investigator:     John S Nelson, M.D,PhD     Beckman Laser Institute Medical Clinic    
  More Information

Responsible Party:   Beckman Laser Institute, University of California, Irvine ( J. Stuart Nelson, M.D., Ph.D. Associate Director and Medical Director at the Beckman Laser Institute and Medical Clinic )
Study ID Numbers:   NIH-LAMMP P41-RR01192
First Received:   January 25, 2008
Last Updated:   January 25, 2008
ClinicalTrials.gov Identifier:   NCT00610402
Health Authority:   United States: Institutional Review Board

Study placed in the following topic categories:
Angiomatosis
Cerebral Infarction
Klippel-Trenaunay-Weber Syndrome
Brain Diseases
Cerebrovascular Disorders
Parkes Weber syndrome
Weber syndrome
Sturge-Weber Syndrome
Abnormalities, Multiple
Hemangioma
Brain Ischemia
Congenital Abnormalities
Skin Diseases, Genetic
Ectodermal Dysplasia
Neurocutaneous Syndromes
Skin Diseases
Stroke
Skin Abnormalities
Vascular Diseases
Central Nervous System Diseases
Sturge-Weber syndrome
Ischemia
Brain Stem Infarctions
Antibodies
Ectodermal dysplasia
Genetic Diseases, Inborn
Klippel Trenaunay Weber syndrome
Brain Infarction
Infarction
Ectodermal dysplasias

Additional relevant MeSH terms:
Neoplasms
Pathologic Processes
Disease
Neoplasms by Histologic Type
Syndrome
Nervous System Diseases
Neoplasms, Vascular Tissue
Cardiovascular Diseases

ClinicalTrials.gov processed this record on July 18, 2008




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