By InvitationNot Applicable

Longitudinal Study of a Bionic Eye

Australia7 participantsStarted 2021-12-09

Plain-language summary

This is a longitudinal observational study with participants who have been implanted with the suprachoroidal retinal prosthesis.

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

What they're measuring

Effectiveness of vision processing method in the laboratory.

Timeframe: 5 years.

Effectiveness of vision processing method in the 'real world' featured environment.

Timeframe: 5 years.

Trial details

NCT IDNCT05158049

SponsorCenter for Eye Research Australia

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-12-09

View on ClinicalTrials.gov More Retinitis Pigmentosa trials