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Corrected VA With Long-Term Follow-Up After AcrySof® Intraocular Lens (IOL) Implantation

NCT02450799 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 104

Last updated 2016-12-09

Study results available
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Summary

The purpose of this study is to compare the long-term visual acuity (VA) with an acrylic IOL to a silicone or polymethylmethacrylate (PMMA) IOL in cataract patients. This study will take place in Japan.

Conditions

  • Pseudophakia

Interventions

DEVICE

Acrylic IOL

Acrylic IOL for long-term implantation in the cataract patient

DEVICE

Silicone IOL

Silicone IOL for long-term implantation in the cataract patient

DEVICE

PMMA IOL

Polymethylmethacrylate IOL for long-term implantation in the cataract patient

Sponsors & Collaborators

  • Alcon, a Novartis Company

    lead INDUSTRY

Principal Investigators

  • Group Manager, Clinical Dev. · Alcon Japan, Ltd.

Study Design

Allocation
NON_RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2016-05-31
Completion
2016-05-31

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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 NCT02450799 on ClinicalTrials.gov