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Clinical Study to Compare Visual Performance of Two Trifocal IOLs

NCT03347981 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 53

Last updated 2021-05-06

No results posted yet for this study

Summary

Prospective, randomised, controlled, single-surgeon, single-center post-market clinical follow up study to compare the clinical outcomes of two trifocal IOLs with different material

Conditions

Interventions

DEVICE

IOL implantation experimental

Implantation of trifocal IOL POD F GF consisting of hydrophobic material

DEVICE

IOL implantation active comparator

Implantation of trifocal IOL POD F consisting of hydrophilic material

Sponsors & Collaborators

  • Beaver-Visitec International, Inc.

    lead INDUSTRY

Principal Investigators

  • Francisco Poyales Galan, MD · Innova Ocular IOA Madrid

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-10-02
Primary Completion
2019-05-21
Completion
2019-05-21

Countries

  • Spain

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 NCT03347981 on ClinicalTrials.gov