Evaluation of Cataract Surgery Outcomes in Patients With Prior Laser Vision Correction Implanted With the CT LUCIA Lens

Exclusion Criteria

• •1. Implantation of an IOL other than the CT LUCIA 621P in one or both eyes.
• •2. Eyes with preoperative anterior corneal astigmatism of ΔTK ≥1.00 D as measured by the IOLMaster 700 or with greater than 0.75 D predicted post-operative astigmatism at the spectacle plane.
• •3. Visual field loss which has an impact on visual acuity.
• •4. Subjects with diagnosed degenerative visual disorders (e.g., macular degeneration or other retinal disorders) that would confound visual acuity measurement.
• •5. Subjects with surgical complications in whom a CT LUCIA 621P IOL cannot be implanted in either eye.
• •6. Eyes with irregular corneal astigmatism, epithelial basement membrane dystrophy, chronic dry eye requiring continual treatment, underwent more than one LVC procedure in one or both eyes, or complications from the previous LVC which required additional surgical intervention.
• •7. Subjects with planned ocular surgery during the study (except Nd:YAG capsulotomy is permitted).
• •8. History of acute or chronic disease, pathology, illness, or ocular trauma that would, in the opinion of the investigator, confound results.
• •9. Current diagnosis of macular degeneration, cystoid macular edema, proliferative diabetic retinopathy, amblyopia, or other chronic ocular conditions that would confound the study results.
• •10. A current diagnosis of moderate or severe glaucoma.
• •11. Patients with strabismus, forme fruste keratoconus, keratoconus or other corneal pathologies that would confound visual acuity measurement.
• •12. Previous radial keratotomy (RK).
• •13. Previous corneal keratoplasty (e.g., corneal transplant, Descemet's stripping automated endothelial keratoplasty (DSAEK), lamellar keratoplasty).
• •14. Previous anterior or posterior chamber surgery (e.g., vitrectomy, laser iridotomy).
• •15. Pupil abnormalities (non-reactive, tonic pupils, abnormally shaped pupils, or pupils that do not dilate under mesopic/scotopic conditions).
• •16. Capsular or zonular abnormalities or other conditions that may affect the postoperative centration or tilt of the lens (e.g., pseudoexfoliation syndrome).
• •17. Usage of contact lenses during study participation.
• •18. Concurrent participation in another device investigation.