Phacoemulsification and Intraocular Lens Implantation: Patient Registry
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY
The aim of the study is to create a patient registry that will allow for comparison of cataract treatment outcomes using phacoemulsification with implantation of different types of intraocular lenses.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Patients who have undergone cataract surgery or are scheduled for bilateral cataract surgery with implantation of an extended-depth-of-focus (EDOF) intraocular lens, a monofocal-plus intraocular lens, or a standard monofocal intraocular lens.
Locations
Other Locations
Poland
Sensor Cliniq
RECRUITING
Warsaw
Time Frame
Start Date: 2025-01-02
Estimated Completion Date: 2026-07
Participants
Target number of participants: 300
Treatments
Bilateral Monofocal IOL
Patients who underwent bilateral cataract surgery with implantation of monofocal intraocular lenses in both eyes between 2021 and 2025, and attended a follow-up visit.
Bilateral Monofocal-plus IOL
Patients who underwent bilateral cataract surgery with implantation of monofocal-plus intraocular lenses in both eyes between 2021 and 2025, and attended a follow-up visit.
Bilateral EDOF IOL
Patients who underwent bilateral cataract surgery with implantation of extended-depth-of-focus (EDOF) intraocular lenses in both eyes between 2021 and 2025, and attended a follow-up visit.
Related Therapeutic Areas
Sponsors
Leads: Sensor Cliniq