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Intraocular Implant

Single Arm Treatment. for Presbyopia

Phase 4
Waitlist Available
Led By Mark E. Whitten, MD
Research Sponsored by Whitten Laser Eye
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights

Study Summary

The objective of this study is to evaluate the Raindrop® Near Vision Inlay for the improvement of near vision in presbyopes implanted under a corneal flap or within a small-incision pocket.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Uncorrected Visual Acuity
Secondary outcome measures
Arcus Senilis

Trial Design

1Treatment groups
Experimental Treatment
Group I: Single Arm Treatment.Experimental Treatment1 Intervention
All patients will be unilaterally implanted in the non-dominant eye with the Raindrop Near Vision Inlay for the compensation of presbyopia.

Find a Location

Who is running the clinical trial?

Whitten Laser EyeLead Sponsor
1 Previous Clinical Trials
40 Total Patients Enrolled
1 Trials studying Presbyopia
40 Patients Enrolled for Presbyopia
Mark E. Whitten, MDPrincipal InvestigatorWhitten Laser Eye

Frequently Asked Questions

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~8 spots leftby Apr 2025