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Biomarker Development in Sturge-Weber Syndrome

NCT01345305 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2020-04-16

No results posted yet for this study

Summary

This is a study of 40 individuals with Sturge-Weber Syndrome (SWS) brain and/or eye involvement. It will examine the test-retest reliability of the following clinical tests:

1. Quantitative EEG
2. Transcranial Doppler
3. Medical Rehabilitation Scales
4. Optical Coherence Tomography

Conditions

  • Sturge-Weber Syndrome

Sponsors & Collaborators

  • National Institutes of Health (NIH)

    collaborator NIH

  • University of California, San Francisco

    collaborator OTHER

  • National Institute of Neurological Disorders and Stroke (NINDS)

    collaborator NIH

  • Hugo W. Moser Research Institute at Kennedy Krieger, Inc.

    lead OTHER

Principal Investigators

  • Anne M Comi, M.D. · Hunter Nelson Sturge-Weber Center

Eligibility

Min Age
6 Months
Max Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-07-31
Primary Completion
2012-11-30
Completion
2012-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01345305 on ClinicalTrials.gov