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Natural History and Genetic Studies of Usher Syndrome
This study is currently recruiting participants.
Study NCT00106743 Information provided by National Institutes of Health Clinical Center (CC)
First Received: March 29, 2005 Last Updated: September 17, 2009
History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Retinitis Pigmentosa Syndromic
Congenital Deafness
Usher Syndrome
Retinitis Pigmentosa and Deafness
Progressive Hearing Loss
Retinitis Pigmentosa
Additional conditions recognized in this trial
Deafness
Hearing Loss
Retinitis
Syndrome
Usher Syndromes
More general conditions related to this trial
Abnormalities, Multiple
Blindness
Congenital Abnormalities
Deaf-Blind Disorders
Disease
Ear Diseases
Eye Diseases
Eye Diseases, Hereditary
Genetic Diseases, Inborn
Hearing Disorders
Hearing Loss, Sensorineural
Nervous System Diseases
Neurologic Manifestations
Otorhinolaryngologic Diseases
Pathologic Processes
Retinal Degeneration
Retinal Diseases
Sensation Disorders
Signs and Symptoms
Vision Disorders
Sponsors listed in this trial
National Eye Institute (NEI)
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