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NCT04907955

Visual Performance Following Implantation of Presbyopia Correcting IOLs

Completed NA Last updated 1 June 2021
What this trial tests

NA trial testing phacoemulsification with implantation of presbyopia correcting IOL in Loss of Visual Contrast Sensitivity in 50 participants. Completed in 30 May 2020.

Timeline
1 June 2019
Primary endpoint
30 May 2020
30 May 2020

Quick facts

Lead sponsorDar Al Shifa Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment50
Start date1 June 2019
Primary completion30 May 2020
Estimated completion30 May 2020
Sites1 location across Kuwait

Drugs / interventions tested

Conditions studied

Sponsor

Dar Al Shifa Hospital

Who can join

Eligibility, any sex, with Loss of Visual Contrast Sensitivity or Near Vision. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Trifocal intraocular lenses versus bifocal intraocular lenses after cataract extraction among participants with presbyopia.
    Zamora-de La Cruz D, Bartlett J, Gutierrez M, Ng SM. · · 2023 · cited 20× · PMID 36705482 · DOI 10.1002/14651858.cd012648.pub3
  2. Visual performance following implantation of presbyopia correcting intraocular lenses.
    Torky MA, Nokrashy AE, Metwally H, Abdelhameed AG. · · 2025 · cited 15× · PMID 35941184 · DOI 10.1038/s41433-022-02188-y

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Other Dar Al Shifa Hospital trials

Trials by the same sponsor.

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Data sources for this page

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