Status: Recruiting
Refocus VisAbility™ Micro Insert System Pre-market Clinical Trial
The primary study objective is to evaluate the safety and effectiveness of the VisAbility™ Micro Insert System for improvement in binocular distance corrected near visual acuity in presbyopic patients.
Participants needed: 33
Trial details
Age: 45-60Biological sex: AllType: InterventionalSponsor: Refocus Group, Inc.Updated: Jun 9, 2026Locations: 1
Eligibility criteria
Subjects must be between ages of 45 to 60 at the time of enrolment. [+3]
Subjects where either pupil has a baseline percent change from scotopic to photo... [+3]