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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01062672
Other study ID # H--22516
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 2009
Est. completion date December 2015

Study information

Verified date April 2022
Source Baylor College of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study's objective is to measure changes in human visual cortex organization that may arise as a result of injury to the visual pathways. Subjects with retinal or cortical injury will be studied and compared to appropriate controls. Functional magnetic resonance imaging methods are used to monitor cortical topography in time. The main aims of the study are to determine: 1) what are the patterns of cortical reorganization that are seen spontaneously after injury, and 2) whether rehabilitative training can promote adaptive reorganization enhancing recovery.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Stable lesion of the visual pathways resulting in a visual field scotoma. Exclusion Criteria: - Inability to undergo magnetic resonance imaging, - Inability to comply with basic instructions, - Inability to perform the behavioral tasks required, - Patients with chronic progressive neurological or psychiatric disorders, - Patients that are pregnant, or breast feeding.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Max Planck Institute for Biological Cybernetics Tuebingen
United States Baylor College of Medicine Houston Texas

Sponsors (2)

Lead Sponsor Collaborator
Baylor College of Medicine Brigham and Women's Hospital

Countries where clinical trial is conducted

United States,  Germany, 

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