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Refocus VisAbility™ Micro Insert System Pre-market Clinical Trial
Sponsor: Refocus Group, Inc.
Summary
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.
Official title: A Prospective, Multicenter Clinical Trial To Evaluate The Safety And The Improvement In Near Visual Acuity In Presbyopic Patients Treated With The VisAbility™ Micro Insert System Through 12 Months
Key Details
Gender
All
Age Range
45 Years - 60 Years
Study Type
INTERVENTIONAL
Enrollment
33
Start Date
2026-06-02
Completion Date
2027-12
Last Updated
2026-09-10
Healthy Volunteers
No
Conditions
Interventions
VisAbility™ Micro Insert System
Surgeon will proceed to VisAbility™ Micro Insert System treatment.
Locations (2)
Refocus Clinical Site
Bochum, Germany
Universitäts-Augenklinik Heidelberg
Heidelberg, Germany