Phacoemulsification and Intraocular Lens Implantation: Patient Registry
Recruiting now
Conditions studied: Cataract, Intraocular Lens
In brief
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.
Key facts
- Study ID
- NCT07276217
- Run by
- Sensor Cliniq
- People needed
- 300
- Starts
- 2025-01-02
- Expected to finish
- 2026-07-01
- Last updated by the study team
- 2025-12-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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 may not qualify if…
- 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
Where it is running
- Sensor Cliniq — Warsaw, Poland (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.