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NCT00106743 · ClinicalTrials.gov registry record
Natural History and Genetic Studies of Usher Syndrome
A clinical trial, sponsored by National Eye Institute (NEI).
- Completed
- Registry status
- 249
- Enrollment target
NCT00106743 is a clinical trial that has completed, run by National Eye Institute (NEI). The registered enrollment target is 249 participants.
The verdict
NCT00106743 has completed, sponsored by National Eye Institute (NEI).
- COMPLETED
- Registry status
- 249 participants
- Enrollment target
Study Summary
This study will explore clinical and genetic aspects of Usher syndrome, an inherited disease causing deafness or impaired hearing, visual problems, and, in some cases, unsteadiness or balance problems. Patients with type 1 Usher syndrome usually are deaf from birth and have speech and balance problems. Patients with type 2 disease generally are hearing impaired but have no balance problems. Patients with type 3 disease have progressive hearing loss and balance problems. All patients develop retinitis pigmentosa, an eye disease that causes poor night vision and eventually, blindness. Patients of any age with Usher syndrome may be eligible for this study. Patients who have had eye and hearing evaluations are asked to send their medical records to the research team at the National Eye Institute (NEI) for review. They are also asked to have a blood sample drawn by a medical professional and sent to NEI for genetic analysis. Finally, they are interviewed about their family histories, particularly about other relative with eye disease. Patients who have not been evaluated previously have the following tests and procedures at NIH: * Family medical history, especially regarding eye disease. A family tree is drawn. * Blood draw for genetic studies of Usher syndrome. * Eye examination to assess visual acuity and eye pressure, and to examine pupils, lens, retina, and eye movements. * Electroretinogram (ERG) to test the function of visual cells. Wearing eye patches, the patient sits in a dark room for 30 minutes. Electrodes are taped to the forehead and the eye patches are removed. The surface of the eye is numbed with eye drops and contact lenses are placed on the eyes. The patient looks inside a hollow, dark globe and sees a series of light flashes. Then a light is turned on inside the globe and more flashes appear. The contact lenses sense small electrical signals generated by the retina when the light flashes. * Fluorescein angiography to evaluate the eye's blood vessels.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 249 participants |
| Start Date | 2005-03-21 |
| Est. Completion | 2019-04-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00106743
The ClinicalTrials.gov registry entry for NCT00106743 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 249 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Eye Institute (NEI), which has 221 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 0 interventions.
NCT00106743 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00106743 about?
NCT00106743 is a clinical study titled "Natural History and Genetic Studies of Usher Syndrome". This study will explore clinical and genetic aspects of Usher syndrome, an inherited disease causing deafness or impaired hearing, visual problems, and, in some cases, unsteadiness or balance problems. Patients with type 1 Usher syndrome usually are deaf from birth and have speech and balance proble...
What is the current status of trial NCT00106743?
This trial is currently completed. The enrollment target is 249 participants. The study started on 2005-03-21. Estimated completion is 2019-04-30.
Who is sponsoring clinical trial NCT00106743?
This trial is sponsored by National Eye Institute (NEI), which has 221 total clinical trials registered on ClinicalTrials.gov.
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