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Clinical Evaluation Study for Assessing the Visual Performance of Hanita Lenses Trifocal IOL

NCT04843748 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2021-04-14

No results posted yet for this study

Summary

Hanita Lenses Trifocal IOL, SeeLens AFR (Intensity IOL).Prospective, single-arm single-center, open-label study.

Conditions

  • Cataract

Interventions

DEVICE

cataract surgery and intraocular lens implantation - both eyes

cataract surgery and intraocular lens implantation for both eyes

Sponsors & Collaborators

  • Hanita Lenses

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
45 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-18
Primary Completion
2021-01-06
Completion
2021-01-06

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 NCT04843748 on ClinicalTrials.gov