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RECRUITING
NCT07637500
NA

Refocus VisAbility™ Micro Insert System Pre-market Clinical Trial

Sponsor: Refocus Group, Inc.

View on ClinicalTrials.gov

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

PROCEDURE

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