This is a longitudinal observational study with participants who have been implanted with the suprachoroidal retinal prosthesis.
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Willing to provide signed informed consent;
* Implanted with a suprachoroidal retinal prosthesis;
* Be available for the study visits;
* Willing to comply with study assessments;
* In good general health and mobile.
Exclusion Criteria:
* Medical condition that prohibits mobility;
* Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study.
Primary outcome measure(s)
Effectiveness of vision processing method in the laboratory. — 5 years. Measure effectiveness of of the vision processing method via observational and quantitative data.
Effectiveness of vision processing method in the 'real world' featured environment. — 5 years. Measure the effectiveness of the vision processing method via observational qualitative and quantitative data in participant 'real world' featured environment.
Trial sites (1)
Facility
City
Region
Status
Centre for Eye Research Australia
Melbourne E.
Victoria
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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