The VIS Opti-K Low Vision Aid Device Provides Vision Improvement.

Part of paid clinical trials in Austin, Texas.

Sponsor
VIS, Inc.
Study ID
NCT06597292
Status
Not Yet Recruiting

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Conditions

  • Hyperopia
  • Presbyopia

Eligibility Criteria

Sex
ALL
Age
40 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Vision improvement — DEVICE
    Vision improvement for patients with refractive disorders (hyperopia and presbyopia)

Study Details

The VIS Opti-K Low Vision Aid device will be used to provide vision improvement to patients with refractive disorders (hyperopia and presbyopia).

Key Dates

Start date
Sep 16, 2024
Status verified
Sep 2024
Primary completion
Sep 30, 2026
Completion
Dec 30, 2026

Study Design

Enrollment
200 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Vision improvement

Primary Outcome Measure

Uncorrected Distance Visual Acuity (UDVA) [ Time Frame: Up to 24 months post-treatment ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
VIS, Inc.AustinTexas78731
Michael Berry, PhD
[email protected]
831-869-1384

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By research site
VIS, Inc.· Austin, TX

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