Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Nil: Nil
Intervention2: Nil: Nil
Control Intervention1: Nil: Nil
Sponsors
Bhaktivedanta Hospital and Research Institute
Eligibility
Inclusion criteria
Inclusion criteria: Undergone bilateral implantation with Johnson and Johnson Tecnis Eyhance enhanced monofocal IOL. Willingness to undergo minimum follow up period of 1 month after second eye cataract surgery. Pre Op corneal astigmatism less than/equal to 0.75D
Exclusion criteria
Exclusion criteria: Age 20-80 Years except cataract History of trauma or previous ocular surgery. Axial length over 25mm Pre-existing corneal pathology. Glaucoma or optic neuropathy. Diabetic retinopathy or macular degeneration. • Systemic conditions affecting neuro-ocular pathways. • Intra-operative complications (e.g. posterior capsular rupture, IOL outside the bag)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate visual and refractive outcomes, as well as patient satisfaction after bilateral implantation of an enhanced monofocal intraocular lens (Eyhance IOL - Johnson and Johnson vision) with emmetropia as a target refraction.Timepoint: Day1, Day7, Day15, 1 Month. | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare visual outcomes with preoperative parameters and with established data from conventional monofocal IOLs. To assess the extent of spectacle independence achieved by the patients for various visual functions and activities of daily living using Catquest-9SF questionnaire. To assess the impact of various pupillary diameters in mesopic and photopic conditions on the intermediate visual acuity. To evaluate contrast sensitivity under photopic and mesopic conditions. To evaluate the Defocus curve - in uniocular and binocular conditions. Timepoint: Day1, Day7, Day15, 1 Month. | — |
Countries
India
Contacts
Public ContactDr Shubham Vivek Naik
Bhaktivedanta hospital and research institute
Outcome results
None listed