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Pilot Study With a Diffractive Trifocal IOL (POD AY 26P FineVision)

NCT02042755 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 19

Last updated 2021-05-06

No results posted yet for this study

Summary

The principal objective of the study is to determine the visual acuity at far, intermediate and near distances tested with optotypes at different distances from the eyes and tested with defocus addition lenses of patients implanted bilaterally with the POD 26P AY FineVision.

Secondary objective will be to test the glare and contrast sensitivity.

Conditions

  • Bilateral Cataract

Interventions

DEVICE

trifocal intraocular lens

Standard cataract surgery

Sponsors & Collaborators

  • Beaver-Visitec International, Inc.

    lead INDUSTRY

Principal Investigators

  • Irit Bahar, MD · Rabin Medical Center

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-02-28
Primary Completion
2016-05-31
Completion
2016-05-31

Countries

  • Israel

Study Locations

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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 NCT02042755 on ClinicalTrials.gov