Visual Outcomes and Patient Satisfaction With Implantation of the Clareon Monofocal IOL With the New Clareon Manual Monarch IV IOL Delivery System

Eye Consultants of Atlanta

Status

Completed

Conditions

Cataract

Treatments

Device: Clareon monofocal Intraocular lens (toric and non-toric models)

Study type

Observational

Funder types

Other

Industry

Identifiers

NCT05526781

JC-22-001

Details and patient eligibility

About

To evaluate visual outcomes, in-the-bag placement and patient satisfaction in patients implanted with either Clareon monofocal or Clareon monofocal toric IOLs with the Monarch IV inserter and targeted for emmetropia.

Full description

This study is a single-arm clinical evaluation study of visual performance and patient satisfaction, after successful bilateral cataract surgery. Subjects will be assessed pre- operatively, operatively and at 1 month and 3 months post-operatively. Clinical evaluations will include measurement of bilateral visual acuity, manifest refraction, and IOLSAT questionnaire.

Enrollment

34 patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects are eligible for the study if they meet the following criteria: Note: Ocular criteria must be met in both eyes.

Adult cataract surgical patients over the age of 45 with visually significant bilateral cataracts (glare visual acuity 20/40 or worse with BCVA testing), with planned cataract extraction using phacoemulsification, clear corneal incision and Clareon monofocal or Clareon toric with Monarch IV.
Able to provide written informed consent for participation in the study.
All eyes will be in the range of availability for Clareon monofocal and Clareon toric with Monarch IV.
Expected visual potential of 20/25 Snellen (0.10 logMAR) or better in each eye.

Exclusion criteria

If any of the following exclusion criteria are applicable to the subject or either eye, the subject should not be enrolled in the study.

Visually significant co-morbidities (corneal, retina, optic nerve disease) that could affect their satisfaction with surgery.
History of neovascular AMD, diabetic macular edema, unstable proliferative diabetic retinopathy, geographic atrophy, branch retinal artery or branch retinal vein occlusion, central retinal artery or central retinal vein occlusion, moderate to severe epiretinal membrane, severe dry eye.
History of intraocular infection including HSV keratitis, VZV keratitis, endophthalmitis.
History of previous ocular surgery, including corneal refractive surgery, eye trauma or retinal detachment surgery.
History of rheumatoid arthritis, ocular cicatricial pemphigoid, or Steven's Johnson Syndrome.
History of glaucoma.

The principal investigator reserves the right to declare a patient ineligible or non- evaluable based on medical evidence that indicates they are unsuitable for the trial.

Pregnancy has a known effect on the stability of refractions and visual acuity. As such, subjects who become pregnant during the study will not be discontinued but their data may be excluded from analyses of effectiveness.