RECRUITINGOBSERVATIONAL
Phacoemulsification and Intraocular Lens Implantation: Patient Registry
About This Trial
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.
Who May Be Eligible (Plain English)
Who May Qualify:
- 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.
Who Should NOT Join This Trial:
- 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 0.5
- Intraoperative complications, including posterior capsule rupture
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* 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.
Exclusion Criteria:
* 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 0.5
* Intraoperative complications, including posterior capsule rupture
Treatments Being Tested
DEVICE
Intraocular lens
Implantation of an intraocular lens following phacoemulsification cataract extraction, with lens type selected according to routine clinical practice (e.g., monofocal, toric, multifocal, or extended-depth-of-focus).
Locations (1)
Sensor Cliniq
Warsaw, Poland