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Experimental and Clinical Studies of Retinal Stimulation

NCT03635645 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2022-12-14

No results posted yet for this study

Summary

The study will evaluate new methods of retinal stimulation and training with the goal of improving the visual ability of retinal prosthesis participants.

Conditions

Interventions

DEVICE

New visual processing unit (VPU) with asymmetric waveforms

A VPU will apply asymmetric and symmetric stimulation pulses.

DEVICE

New VPU with bipolar stimulation

A VPU will apply bipolar stimulus pulses.

Sponsors & Collaborators

Principal Investigators

  • James Weiland · University of Michigan

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
25 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-30
Primary Completion
2023-10-30
Completion
2023-10-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03635645 on ClinicalTrials.gov