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Active Not RecruitingNCT04676854

Restoration of Central Vision With the PRIMA System in Patients With Atrophic AMD

Restoration of Central Vision With the PRIMA System in Patients With Atrophic Age-Related Macular Degeneration

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
38 (estimated)
Sponsor
Science Corporation · Industry
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate the efficacy and safety of the PRIMA System in patients with atrophic AMD. Eligible subjects will be implanted with the PRIMA Implant. The subjects will be assessed with various visual function and functional vision tests at defined timepoints throughout the clinical investigation with the PRIMA System (Implant and Visual Processor).

Conditions

Interventions

TypeNameDescription
DEVICEPRIMA Bionic Vision SystemImplantation of PRIMA, Vision training, follow up

Timeline

Start date
2020-11-24
Primary completion
2024-02-01
Completion
2028-02-01
First posted
2020-12-21
Last updated
2024-11-29

Locations

21 sites across 6 countries: France, Germany, Italy, Netherlands, Spain, United Kingdom

Source: ClinicalTrials.gov record NCT04676854. Inclusion in this directory is not an endorsement.

Restoration of Central Vision With the PRIMA System in Patients With Atrophic AMD (NCT04676854) · Clinical Trials Directory