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Comparing Visual Outcomes in Matched Patients Receiving a Low Cylinder Power Toric IOL or a Non-toric IOL

NCT06717607 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 43

Last updated 2024-12-05

No results posted yet for this study

Summary

The purpose of the study is to determine if visual function is improved with implantation of a low-cylinder toric intraocular lens, relative to a non-toric intraocular lens.

Conditions

  • Cataract and IOL Surgery

Interventions

DEVICE

low cylinder toric IOL

Clareon T2 toric IOL implantation

DEVICE

non-toric IOL implantation

Clareon non-toric IOL

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • Ifocus Oyeklinikk

    lead NETWORK

Principal Investigators

  • Kjell Gunnar Gundersen, MD, PhD · Ifocus Oyeklinikk

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-08-20
Primary Completion
2024-08-30
Completion
2024-08-30
FDA Device
Yes

Countries

  • Norway

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 NCT06717607 on ClinicalTrials.gov