Trials / Completed
CompletedNCT06717607
Comparing Visual Outcomes in Matched Patients Receiving a Low Cylinder Power Toric IOL or a Non-toric IOL
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 43 (actual)
- Sponsor
- Ifocus Oyeklinikk · Network
- Sex
- All
- Age
- 40 Years
- Healthy volunteers
- Accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | low cylinder toric IOL | Clareon T2 toric IOL implantation |
| DEVICE | non-toric IOL implantation | Clareon non-toric IOL |
Timeline
- Start date
- 2022-08-20
- Primary completion
- 2024-08-30
- Completion
- 2024-08-30
- First posted
- 2024-12-05
- Last updated
- 2024-12-05
Locations
1 site across 1 country: Norway
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06717607. Inclusion in this directory is not an endorsement.