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Clareon Toric Study (T2-T9)

Corneal Astigmatism | Aphakia

The purpose of this post-market study is to describe the long-term safety and performance of Clareon Toric Intraocular Lenses (IOLs).

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

Key Inclusion Criteria:

* Able to understand and sign the informed consent form.
* Willing and able to attend all scheduled study visits as required per protocol.
* Cataract in one or both eyes with planned extraction by conventional phacoemulsification.
* Astigmatism in the operative eye(s).
* Other protocol-defined inclusion criteria may apply.

Key Exclusion Criteria:

* Women of childbearing potential, currently pregnant, intend to become pregnant during the study, or nursing.
* History of retinal detachment, age-related macular degeneration, glaucoma, diabetic retinopathy, or any pathologic changes associated with the optic nerve.
* Clinically significant corneal disease that may, according to the Investigator's medical opinion, adversely affect visual outcomes.
* Clinically significant dry eye that would affect study measurements based on the Investigator's expert medical opinion.
* History of prior intraocular or corneal surgery.
* Other protocol-defined exclusion criteria may apply.

Lieu de l'étude

Uptown Eye Specialists
Uptown Eye Specialists
Concord, Ontario
Canada

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McGill University
McGill University
Montréal, Quebec
Canada

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Gimbel Eye Centre
Gimbel Eye Centre
Calgary, Alberta
Canada

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Bellevue
Bellevue
Montréal, Quebec
Canada

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Prism Eye Institute
Prism Eye Institute
Oakville, Ontario
Canada

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Laurentians Eye Institute
Laurentians Eye Institute
Boisbriand, Quebec
Canada

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Étude parrainée par
Alcon Research
Participants recherchés
Plus d'informations
ID de l'étude: NCT06285695