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Visual Performance Following Implantation of Presbyopia Correcting IOLs

NCT04907955 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2021-06-01

No results posted yet for this study

Summary

The purpose of the current study was to compare the visual performance after bilateral implantation of the Panoptix IOL , or the AT LISA IOL or Tecnis Symfony IOL . The focus was on intermediate vision, defocus curves, and contrast sensitivity.

Conditions

  • Loss of Visual Contrast Sensitivity
  • Near Vision
  • Visual Impairment

Interventions

PROCEDURE

phacoemulsification with implantation of presbyopia correcting IOL

cataract extraction with phacoemulsification and insertion of presbyopia correcting IOL

Sponsors & Collaborators

  • Dar Al Shifa Hospital

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-01
Primary Completion
2020-05-30
Completion
2020-05-30

Countries

  • Kuwait

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 NCT04907955 on ClinicalTrials.gov