A Phase I Feasibility Study of an Intracortical Visual Prosthesis (ICVP) for People With Blindness

Optic Nerve Diseases Clinical Trial

— ICVP  

Official title:

ICVP - A Phase I Clinical Trial to Determine the Feasibility of a Human Cortical Visual Prosthesis for People With Blindness

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04634383
• Other study ID #: ICVP0001
• Secondary ID: UH3NS095557
• Status: Recruiting
• Phase: N/A
• Start date: August 20, 2020
• Est. completion date: August 31, 2023

Study information

• Verified date: January 2022
• Source: Illinois Institute of Technology
• Contact: Recruitment Director
• Phone: 312-567-5304
• Email: ICVP[@]iit.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 5
• Est. completion date: August 31, 2023
• Est. primary completion date: August 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years to 70 Years

Eligibility

Inclusion Criteria:

• 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.
• 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

Related Conditions & MeSH terms

• Blindness
• Blindness,Acquired
• Nervous System Diseases
• Ocular Injury
• Optic Nerve Diseases
• Photoreceptor Degeneration

Intervention

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.

Locations

Country	Name	City	State
United States	Illinois Institue of Technology	Chicago	Illinois

Sponsors (7)

Lead Sponsor	Collaborator
Illinois Institute of Technology	Johns Hopkins University, National Institute of Neurological Disorders and Stroke (NINDS), Rush University Medical Center, The Chicago Lighthouse, The University of Texas at Dallas, University of Chicago

Country where clinical trial is conducted

United States, 

References & Publications (2)

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. — View Citation

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. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To test the safety of the WFMA-based cortical interface.	Safety is defined as the number of adverse events occurring over the study period due to surgical complications or use of the WFMA device.	From two-weeks post-op to end of device use, up to 3 years.
Secondary	To test the efficacy of the WFMA-based cortical interface	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.	From four-weeks post-op to end of device use, up to 3 years.