VIS Opti-K Vision Improvement for Presbyopes (VIS Opti-K 002)

VIS, Inc.

Status: Active, not recruiting

Conditions: Presbyopia Correction

Study type: Observational

Funder types: Industry

Identifiers

NCT06702020

VIS Opti-K-Presbyopia #002

Details and patient eligibility

About

The VIS Opti-K device and procedure were used to provide vision improvement to patients with presbyopia.

Full description

The VIS Opti-K device was used to irradiate the cornea with light that changed corneal shape.

Enrollment: 135 patients

Sex: All

Ages: 40+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Female or male Any race 40 years of age or older Presbyopia

Exclusion criteria

None