Clinical Trial: Retrospective Clinical Investigation of the Safety and Performance of 640PM Trifocal IOL Implantation in Patients With Cataract and/or Ametropia (Hyperopia, Myopia) and/or Presbyopia
Study Status: Completed
Recruit Status: Completed
Condition:
Cataract
Presbyopia
Hyperopia
Myopia
Pseudophakia
Study Type: Observational
Official Title: Retrospective Clinical Investigation of the Safety and Performance of 640PM Trifocal IOL Implantation in Patients With Cataract and/or Ametropia (Hyperopia, Myopia) and/or Presbyopia
Brief Summary:
The clinical investigation objective is to evaluate safety and performance outcomes of trifocal IOL implantation to improve vision in patients with cataract and/or ametropia (hyperopia, myopia) and/or presbyopia.Retrospective data from preoperative status up to 12 month postoperative status will be collected from patients that were implanted with Medicontur's 640PM intraocular lens:Preoperative status: Preoperative Screening and BaselineSurgery: IOL implantationM1: 1 month +/- 2 weeks postoperative follow-upM3: 3…
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