Trials / Completed
CompletedNCT01731743
Evaluation of Visual Acuity and Patient Satisfaction With AT LISA TRI 839MP Intraocular Lenses
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 107 (actual)
- Sponsor
- Carl Zeiss Meditec AG · Industry
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | AT LISA tri 839MP |
Timeline
- Start date
- 2012-01-01
- Primary completion
- 2013-07-01
- Completion
- 2013-07-01
- First posted
- 2012-11-22
- Last updated
- 2018-01-29
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01731743. Inclusion in this directory is not an endorsement.