CompletedNot Applicable

Visual Acuity After Using A New Monofocal Intraocular Lens Compared To Standard Monofocal Lens

Egypt20 participantsStarted 2021-01-01

Plain-language summary

This is a prospective comparative interventional clinical study, that took place from January 2021 to November 2021. Twenty patients (20) were enrolled in this study 10 patients in each group. It was designed for comparison of uncorrected and best corrected distance and intermediate vision in patients whom implanted with monofocal Tecnis Eyhance or Tecnis 1-piece IOLs.

Who can participate

Age range50 Years – 75 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 aged 50-75 years old undergoing cataract surgery. * Preoperative corneal astigmatism equal to or less than - 1.00 D. * Availability, willingness and sufficient cognitive awareness to comply with examination procedures Exclusion Criteria: * Visual potential of less than 0.63 due to ocular pathologies. * Corneal astigmatism over -1.00 D cylinder. * Pupil abnormalities (non-reactive, tonic pupils, abnormally shaped pupils, or pupils that do not dilate at least 3.5 mm under mesopic/scotopic conditions). * Capsule or zonular abnormalities that would affect postoperative centration or tilt of the lens and pseudoexfoliation syndrome. * Macular degeneration, cystoid macular edema,Diabetic retinopathy, history of uveitis, optic nerve diseases, glaucoma and amblyopia.

What they're measuring

Uncorrected and best-corrected distance, and intermediate visual acuity.

Timeframe: 3 months post operative

Trial details

NCT IDNCT05430295

SponsorKasr El Aini Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-08-01

View on ClinicalTrials.gov More Lenses, Intraocular trials