Actively Recruiting
Phacoemulsification and Intraocular Lens Implantation: Patient Registry
Led by Sensor Cliniq · Updated on 2025-12-10
300
Participants Needed
1
Research Sites
77 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Phacoemulsification and Intraocular Lens Implantation: Patient Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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.
You will not qualify if you...
- Anterior or posterior segment pathologies affecting postoperative visual acuity, including but not limited to: severe dry eye syndrome, corneal dystrophies, uveitis, retinal degenerative changes, glaucoma, or diabetic retinopathy.
- Pseudoexfoliation syndrome
- Keratoconus
- History of laser refractive surgery
- Prior ocular surgery other than cataract surgery
- Amblyopia
- Posterior capsule opacification
- Postoperative best-corrected visual acuity (BCVA) less than 0.5
- Intraoperative complications, including posterior capsule rupture
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sensor Cliniq
Warsaw, Poland
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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