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Techniques for Processing Eyes Implanted With a Retinal Prosthesis for Localized Histopathological Analysis
Published on: August 2, 2013
Second-Generation (44-Channel) Suprachoroidal Retinal Prosthesis: Surgical Stability and Safety During a 2-Year
Penelope J Allen1,2,3, Maria Kolic1, Elizabeth K Baglin1
1Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, Melbourne, Victoria, Australia.
The suprachoroidal retinal prosthesis (ScRP) is safe for retinitis pigmentosa patients, showing stability and minimal adverse events over two years. This indicates feasibility for future clinical studies.
Area of Science:
- Ophthalmology
- Biomedical Engineering
- Neuroscience
Background:
- Retinitis pigmentosa (RP) causes progressive vision loss.
- Current treatments for advanced RP are limited.
- The suprachoroidal retinal prosthesis (ScRP) offers a potential vision restoration strategy.
Purpose of the Study:
- To evaluate the safety and stability of the suprachoroidal retinal prosthesis (ScRP).
- To assess the long-term outcomes of ScRP implantation in patients with retinitis pigmentosa (RP).
Main Methods:
- A prospective, single-arm clinical trial involving four participants with advanced RP.
- Unilateral implantation of a 44-channel ScRP.
- Monitoring for adverse events, implant stability, and functionality over 2.0-2.7 years.
Main Results:
- Surgical implantation was uncomplicated with uneventful recovery.
- No serious adverse events were reported; adverse events were mild.
- The ScRP demonstrated high electrode functionality and acceptable stability with minor initial array movement.
Conclusions:
- Suprachoroidal implantation of the ScRP is safe and well-tolerated in RP patients.
- The device shows minimal long-term impact on ocular structures.
- Findings support the feasibility of the ScRP approach for vision restoration in RP.
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