Condition: Presbyopia · Sponsor: Refocus Group, Inc.
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.
This description comes directly from the study's public registry record.
Safia Ayachi · +3388308811 · safia@medevise-consulting.com
Always discuss trial participation with your own doctor first.
| Universitäts-Augenklinik Heidelberg | Heidelberg, Germany | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07637500