Status:
COMPLETED
Age-Related Macular Degeneration (AMD) - Usability Study
Lead Sponsor:
Notal Vision Ltd.
Conditions:
Age Related Macular Degeneration
Eligibility:
All Genders
50+ years
Brief Summary
The purpose of this study is to evaluate the usability of the Foresee Home device with intermediate AMD patients.
Detailed Description
The AMD usability study is a prospective, longitudinal, multi-center, observational study of patients diagnosed with intermediate (dry) AMD who have been asked by their doctor to use the ForeseeHomeTM...
Eligibility Criteria
Inclusion
- Inclusion criteria
- Subjects diagnosed as intermediate AMD in at least one eye
- Visual Acuity (VA) with habitual correction \<20/60 in the study eye
- Qualified in the clinic to use the device
- Ability to speak, read and understand instructions in English
- Subjects with ability to comprehend and sign the informed consent/authorization
- Exclusion criteria
- Evidence of macular disease other than AMD or glaucoma in the study eye
- Presence of any significant media opacity that precludes a clear view of the macular area as identified in the study eye by biomicroscopy
- Any non-macular related ocular surgery performed within 3 months prior to study entry in the target eye
Exclusion
Key Trial Info
Start Date :
September 1 2009
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 1 2010
Estimated Enrollment :
54 Patients enrolled
Trial Details
Trial ID
NCT00963339
Start Date
September 1 2009
End Date
September 1 2010
Last Update
September 23 2010
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