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NCT05317728
Clinical Study of a Fluid Accommodating Intraocular Lens (IOL) Design
Conditions: Cataract
Sex: All
Ages: 22 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 175
Sponsor: Alcon Research
Location: Clinica 20/20 San José
Summary
The purpose of this clinical study is to evaluate the surgical, refractive, and visual outcomes with implantation of an investigational intraocular lens (IOL).
Eligibility Criteria
Key Inclusion Criteria:
* Able to understand and sign an Institutional Review Board / International Ethics Committee approved informed Consent form;
* Willing and able to attend all scheduled study visits as required by the protocol;
* Diagnosed with bilateral cataracts requiring removal by phacoemulsification with a clear corneal incision;
* Other protocol-specified inclusion criteria may apply.
Key Exclusion Criteria:
* Subjects taking medications that may affect accommodation;
* Clinically significant eye abnormalities as specified in the protocol;
* Previous eye surgery as specified in the protocol;
* Other protocol-specified exclusion criteria may apply.
Source: ClinicalTrials.gov (NCT05317728). StuddyBuddy aggregates publicly available trial information.
