NCT01731743
Completed
Not Applicable
Evaluation of Visual Acuity and Patient Satisfaction With AT LISA TRI 839MP Intraocular Lenses
ConditionsCataract
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cataract
- Sponsor
- Carl Zeiss Meditec AG
- Enrollment
- 107
- Locations
- 1
- Primary Endpoint
- Intermediate visual acuity
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
The purpose of the study is to evaluate the far, intermediate and near visual acuities with a trifocal IOL.
Detailed Description
After bilateral cataract surgery, monocular and binocular uncorrected (UCVA) and best distance corrected visual acuity (BCVA) will be measured at far (4m), intermediate (80 cm) and near (40 cm) distance as well as the subjective refraction. A patient questionnaire will be used to assess the patient satisfaction and spectacle independence.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Man or woman, over 50 years of age
- •Bilateral implantation of a trifocal intraocular lens
- •Capsular bag implantation
Exclusion Criteria
- •Existing ocular pathology
- •Surgical complications
- •Corneal astigmatism ≥ 1.0D
Outcomes
Primary Outcomes
Intermediate visual acuity
Time Frame: up to 3 months postoperatively
Monocular and binocular uncorrected and best distance corrected
Secondary Outcomes
- near and far visual acuity(1 and 3 month postoperatively)
Study Sites (1)
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