Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Alcon Research
The study includes a retrospective chart review for pre-operative, operative, and post-operative data collection, and a prospective, standard-of-care visit to collect study endpoints.
Age
Any age
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subject is implanted with one of the study IOL models between 3 and 5 years previously.
Subject follow-up is expected to be possible during the duration of the study.
Subject or legally authorized representative must be able to understand and sign the IRB/EC approved Informed Consent form. Minor subjects will complete an Assent Form.
Documented medical history and required pre-operative baseline information is available for retrospective data collection.
You may not be if
Subject is participating in a separate investigational drug or device study.
Pregnancy at the time of enrollment.
Clareo Health | A Real-World Evidence (RWE) Long-Term Follow-Up Study to Assess Outcomes of Alcon Monofocal Intraocular Lenses
