VIS Opti-K Vision Improvement for Presbyopes
Active, not recruiting
- Conditions
- Presbyopia Correction
- Registration Number
- NCT06702020
- Lead Sponsor
- VIS, Inc.
- Brief Summary
The VIS Opti-K device and procedure were used to provide vision improvement to patients with presbyopia.
- Detailed Description
The VIS Opti-K device was used to irradiate the cornea with light that changed corneal shape.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 135
Inclusion Criteria
Female or male Any race 40 years of age or older Presbyopia
Exclusion Criteria
None
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Uncorrected distance and near visual acuities Up to 24 months post-treatment Uncorrected distance and near visual acuities are measured using ETDRS or similar charts.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular pathways mediate corneal remodeling after VIS Opti-K irradiation in presbyopia?
How does VIS Opti-K compare to multifocal lenses in presbyopia correction efficacy and safety?
Which corneal biomarkers predict response to VIS Opti-K treatment in presbyopic patients?
What are the long-term adverse events of corneal irradiation using VIS Opti-K in presbyopia?
Are there combination therapies with VIS Opti-K and corneal cross-linking for enhanced presbyopia correction?