Condition: Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction · Sponsor: Carl Zeiss Meditec AG
This is a prospective, Phase IV, post-approval observational study evaluating postoperative outcomes in patients with a history of myopic corneal laser vision correction (LVC) undergoing bilateral cataract surgery with implantation of the CT LUCIA 621P intraocular lens (IOL). Up to 30 subjects (60 eyes) will be enrolled across up to three U.S. investigational sites. The study will assess visual and refractive outcomes, including biometry, manifest refraction, and patient-reported visual function over a 3-month follow-up period.
This description comes directly from the study's public registry record.
Henry Heering · 949-293-0520 · henry.heering@zeiss.com
Always discuss trial participation with your own doctor first.
| Berkeley Eye Center | Sugar Land, Texas, United States | Recruiting |
| Piedmont Eye Center | Lynchburg, Virginia, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07084545