Comparing Visual Outcomes in Matched Patients Receiving a Low Cylinder Power Toric IOL or a Non-toric IOL
- Conditions
- Cataract and IOL Surgery
- Registration Number
- NCT06717607
- Lead Sponsor
- Ifocus Oyeklinikk
- Brief Summary
The purpose of the study is to determine if visual function is improved with implantation of a low-cylinder toric intraocular lens, relative to a non-toric intraocular lens.
- Detailed Description
The Clareon(R) T2 IOL and the Clareon (R) non-toric IOL will be randomly implanted in subjects determined to be appropriate for the T2 IOL. Visual acuity, low contrast acuity and contrast sensitivity will be measured 3 months postoperatively.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 43
- candidate for cataract surgery, suitable for implantation with a low cylinder toric IOL
- pathology that would confound outcomes, previous ocular surgery
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Uncorrected distance visual acuity (UDVA) 3 months UDVA (logMAR)
- Secondary Outcome Measures
Name Time Method Photopic contrast sensitivity 3 months Contrast sensitivity curve
Low contrast visual acuity 3 months Visual acuity (VA), logMAR
Mesopic contrast sensitivity 3 months Contrast sensitivity curve
Mean refraction, spherical equivalent (MRSE) 3 months MRSE, diopters
Manifest refractive cylinder 3 months Manifest cylinder, diopters
Percentage of eyes with <= 0.25 D of refractive cylinder 3 months As above
Percentage of eyes with <= 0.50 D of refractive cylinder 3 months As above
Corrected distance visual acuity 3 months CDVA, logMAR
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (1)
Ifocus øyeklinikk
🇳🇴Haugesund, Norway