Registry of cataract surgery outcomes after phacoemulsification with different intraocular lenses.
Official title: Phacoemulsification and Intraocular Lens Implantation: Patient Registry
Run by Sensor Cliniq · NCT07276217 · Data updated 2026-11-12
This project will collect data to see how people who have phacoemulsification do with different types of intraocular lenses.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 300 (estimated) |
| Sponsor | Sensor Cliniq Academic / other |
| Locations | 1 site (Warsaw) |
| Status | Recruiting |
| Started | January 2, 2025 |
| Main results expected | July 2026 |
| Study ends | July 2026 |
| Registry record updated | December 10, 2025 |
| Trial ID | NCT07276217 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Patients who have had or are scheduled for bilateral cataract surgery with implantation of an EDOF, monofocal-plus, or standard monofocal intraocular lens are eligible.
✕Probably not a fit
Patients with significant anterior or posterior segment disease (for example severe dry eye, corneal dystrophy, uveitis, retinal degeneration, glaucoma, or diabetic retinopathy), pseudoexfoliation, keratoconus, prior laser refractive or other ocular surgery (except cataract), amblyopia, posterior capsule opacification, postoperative BCVA < 0.5, or intraoperative complications are excluded and therefore unlikely to benefit from this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This registry will compile retrospective and prospective clinical data on patients undergoing phacoemulsification with implantation of EDOF, monofocal-plus, or standard monofocal intraocular lenses. Retrospective data will include routinely collected preoperative, intraoperative, and postoperative information, while prospective follow-up will capture visual acuity, refraction, exam findings, patient-reported outcomes, and complications. Patients will be followed for up to 60 months after surgery to compare outcomes across lens types and time points. The registry aims to enable real-world comparisons of safety, visual performance, and patient experience associated with different IOL technologies.
Why it matters
Potential benefit: If successful, the registry could help surgeons and patients choose the intraocular lens type most likely to give better vision and fewer complications.
How similar studies have gone: Comparable registries and comparative studies of intraocular lens types have provided useful information, though long-term comparative data for newer EDOF and monofocal-plus lenses remain somewhat limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
-
Sensor Cliniq
Warsaw, Poland Recruiting
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
IOL with a Virtual Aperture for clearer near and distance vision after cataract surgery
A device study tests whether a virtual aperture intraocular lens can help adults with cataracts see clearly at distances and near without glasses.
-
Rotational Stability of the Acunex Vario Toric
This study tests whether the Acunex Vario toric extended-depth-of-focus intraocular lens stays stable in rotation and effectively reduces astigmatism for people undergoing cataract surgery.
-
Anterior segment anatomy assessment with swept-source OCT in eye surgery patients
This study tests whether swept-source OCT can detail front-eye anatomy in patients undergoing anterior segment eye surgery.
-
MiLOOP-assisted cataract surgery for dense cataracts
In people with dense cataracts, this study tests whether using the miLOOP device during cataract surgery can protect corneal cells and reduce ultrasound energy, compared with standard surgery.
-
Ultrasound check of IOL tilt after cataract surgery
A noninvasive ultrasound test is used to see if an intraocular lens tilts or decentrates after cataract surgery in adults.
-
Visual adaptation and quality of life after different IOL implantation options
This study follows adults who have cataracts and receive bilateral multifocal or mixed IOLs to see how their vision and daily life improve over 6 months.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.