An observational study in Cataract and Intraocular Lens, sponsored by Sensor Cliniq. Recruiting at 1 site in Poland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-12-10.
Sponsored by Sensor Cliniq · Observational
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.
This study will establish a registry to evaluate outcomes associated with intraocular lens implants in patients undergoing cataract surgery. Retrospective assessments will include routinely collected preoperative, intraoperative, and postoperative data. Prospectively, visual acuity, refraction, examination findings, patient-reported outcomes, and complications will be collected for up to 60 months after surgery.
1,701 studies on the registry are indexed under Cataract; 230 are open to participants now.
This study's planned enrollment of 300 is above the median of 81 across 484 observational studies indexed under Cataract.
Browse Cataract studies →This is the only study on the registry with Sensor Cliniq as lead sponsor.
Counted across the registry records on this site, refreshed daily.
Patients who have undergone or are scheduled for bilateral cataract surgery at Sensor Cliniq between 2021 and 2025.
Exclusion Criteria:
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.
Device: Intraocular lens
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.
Device: Intraocular lens
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.
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).
Corrected and Uncorrected Distance, Intermediate and Near Visual Acuity
Distance, intermediate, and near visual acuity will be measured both uncorrected and corrected using standard ETDRS charts at 4 meters for distance, 66 cm for intermediate, and 40 cm for near visual acuity.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Objective Refraction
Spherical and cylindrical refractive errors will be measured objectively using an autorefractometer.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Subjective Refraction
Spherical and cylindrical refractive errors will be measured subjectively using trial frame glasses and patient responses.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Monocular and Binocular Defocus Curve
Visual acuity will be measured at varying defocus levels under monocular and binocular conditions to assess the range of functional vision. Measurements will be taken in 0.5 D steps from +1.00 D to -2.50 D.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Contrast Sensitivity
Contrast sensitivity will be assessed using the Matrix Perceptix test under photopic light conditions.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Keratometry
Keratometry will be measured using IOLMaster 500 and Pentacam
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Anterior Chamber Depth
Anterior chamber depth will be measured using IOLMaster 500 and Pentacam.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Pupil Size
Pupil diameter will be measured using IOLMaster 500 and Pentacam.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Central Corneal Thickness
Central corneal thickness will be measured using Pentacam.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Anterior Chamber Angle
Anterior chamber angle will be measured using Pentacam.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Primary and Secondary Spherical Aberrations
Primary and secondary spherical aberrations will be measured using Pentacam.
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Patient-Reported Spectacle Independence
Degree of spectacle independence will be assessed using the Patient-Reported Spectacle Independence Questionnaire (PRSIQ).
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Patient-Reported Quality of Vision
Quality of vision will be assessed using the Quality of Vision Questionnaire (QoV).
Time frame: Measured at the follow-up visit up to 60 months after cataract surgery
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
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