CompletedNot Applicable

Registry Study on Intraocular Lenses Manufactured by Teleon Surgical B.V.

Netherlands2,183 participantsStarted 2022-02-01

Plain-language summary

This is a retrospective, observational (Registry) study aiming to collect safety and performance data on the use of intraocular lenses (IOLs) manufactured by Teleon Surgical B.V. according to routine practice.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients older than 18 years * Diagnosis of cataract in at least one eye or seeking clear/refractive lens exchange * Provide consent to retrospective data collection Exclusion Criteria: * Patients younger than 18 years * Patients with congenital primary aphakia or secondary aphakia

What they're measuring

Visual acuity (uncorrected and/or corrected)

Timeframe: Preoperatively to Month 24

Trial details

NCT IDNCT05290870

SponsorTeleon Surgical B.V.

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2024-02-29

View on ClinicalTrials.gov More Aphakia trials