The purpose of this study is to determine the feasibility of producing artificial vision in persons with blindness. Study participants will have wireless electrical stimulators implanted into the cortical vision processing areas of their brains. The ability of the participants to perceive artificial vision in response to electrical stimulation will be assessed.
Full Title of Study: “ICVP – A Phase I Clinical Trial to Determine the Feasibility of a Human Cortical Visual Prosthesis for People With Blindness”
- Study Type: Interventional
- Study Design
- Allocation: N/A
- Intervention Model: Single Group Assignment
- Primary Purpose: Device Feasibility
- Masking: None (Open Label)
- Study Primary Completion Date: August 31, 2023
The objective of this study is to test the safety of the ICVP system and the feasibility of eliciting visual percepts in response to electrical stimulation in persons with blindness. The electrical stimulation is provided by wireless floating microelectrode arrays (WFMAs) that are part of the ICVP system. The WFMAs are implanted in the visual cortex. Five participants will take part in the study and each participant will have multiple WFMA devices implanted in their visual cortex on one side of the brain. After recovery from surgery, participants will begin a series of tests to assess the ability of electrical stimulation to induce visual percepts and how these percepts may provide some measure of artificial vision. Weekly participant testing will occur over a period of one to three years.
- Device: WFMA – wireless floating microelectrode array
- Wirelessly transmitted patterns of electrical stimulation will be delivered to the visual cortex of study participants to generate visual percepts.
Arms, Groups and Cohorts
- Experimental: WFMA Cortical Visual Prosthesis Single-arm Study
- The WFMA is an electronic device that is implanted in the cortical vision processing regions of the brain to produce artificial vision.
Clinical Trial Outcome Measures
- To test the safety of the WFMA-based cortical interface.
- Time Frame: From two-weeks post-op to end of device use, up to 3 years.
- Safety is defined as the number of adverse events occurring over the study period due to surgical complications or use of the WFMA device.
- To test the efficacy of the WFMA-based cortical interface
- Time Frame: From four-weeks post-op to end of device use, up to 3 years.
- Efficacy is defined as establishing a chronic intracortical interface for which the ability to elicit visual percepts in response to electrical stimulation can be demonstrated with stimulus intensities of 16 nanocoulombs per phase or less.
Participating in This Clinical Trial
- No light perception or bare light perception, in each eye in accordance with relevant International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) codes, where the physician has no expectation of improvement through currently approved treatments. – History of normal or near-normal vision, with or without refractive correction, during at least the first 10 years of life. – Adjusted to blindness for at least one year. – History of vision or blindness rehabilitation. – Living within 40 miles from The Chicago Lighthouse (CLH). – Willing and able to meet the time demands of the study with transportation assistance. – Willing to agree to audio and video recording, as specified in the pre-screening consent. – Motivated by altruism, willingness to participate in pioneering science. – Demonstrated support from spouse, family and/or friends. – High or average cognitive and spatial functioning. – Normal structural MRI. – English as preferred language. – Normal decision-making capacity. Exclusion Criteria:
- Poor adjustment to blindness, or vision loss within the last year. – Expectation of vision restoration to pre-blindness level through trial participation. – History of alcohol or drug dependence. – Evidence of prior immune response to an orthopedic implant which caused the implant to be explanted – A disease prognosis of living less than five years. – An implant which would prevent screening using MRI, or a pacemaker, or similar implant. – A history of seizures. – Current suicidal ideation. – Poor decision-making capacity. – Current diagnosis or history of severe mental illness. – Women who are pregnant or plan on becoming pregnant in the duration of the trial. – Hand Motion (HM) vision or better vision, – No Light Perception (NLP) or Light Perception (LP) vision with present OptoKinetic Nystagmus (OKN) – NLP vision with pupil constriction – Patients with Islands of perceivable vision in Goldmann Visual Field or Confrontational visual Field will also be excluded from the study. – Patients with Complete media opacity (complete cornea opacity, very dense cataract) that does not allow visualization of the posterior segment to determine the cause of blindness will be excluded from the study. Only patients with NLP and LP vision without OKN will be included in the study. – Patients with NLP or LP vision since birth will also be excluded from the study, as they may not have fully developed higher visual pathways, including cortical connections
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: 65 Years
Are Healthy Volunteers Accepted: No
- Lead Sponsor
- Illinois Institute of Technology
- National Institute of Neurological Disorders and Stroke (NINDS)
- Provider of Information About this Clinical Study
- Overall Official(s)
- Philip R Troyk, PhD, Principal Investigator, Illinois Institute of Technology
- Overall Contact(s)
- Recruitment Director, 312-567-5304, ICVP@iit.edu
Bak M, Girvin JP, Hambrecht FT, Kufta CV, Loeb GE, Schmidt EM. Visual sensations produced by intracortical microstimulation of the human occipital cortex. Med Biol Eng Comput. 1990 May;28(3):257-9.
Schmidt EM, Bak MJ, Hambrecht FT, Kufta CV, O'Rourke DK, Vallabhanath P. Feasibility of a visual prosthesis for the blind based on intracortical microstimulation of the visual cortex. Brain. 1996 Apr;119 ( Pt 2):507-22.
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