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A Study to Evaluate the Raindrop Near Vision Inlay Under Flap or Within Pocket

NCT03376412 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2017-12-18

No results posted yet for this 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.

Conditions

Interventions

DEVICE

Raindrop Near Vision Inlay

A maximum of 60 consecutive non-dominant eyes will be implanted with the Raindrop Near Vision Inlay.

Sponsors & Collaborators

  • Whitten Laser Eye

    lead OTHER

Principal Investigators

  • Mark E. Whitten, MD · Whitten Laser Eye

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-12-08
Primary Completion
2020-12-31
Completion
2020-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03376412 on ClinicalTrials.gov