Trials / Completed
CompletedNCT00366496
Surgical Outcomes After Routine Cataract Extraction & Implantation of a Conventional or Spheric Intraocular Lens
Comparison of Visual Outcomes, Wavefront Analysis, Contrast Sensitivity and Glare Testing Following Cataract Extraction Between Acrysof Single-Piece IOL and Acrysof WF
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (planned)
- Sponsor
- Medical University of South Carolina · Academic / Other
- Sex
- All
- Age
- 50 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
To determine quality of vision post cataract extraction and intraocular lens (IOL) implantation of 2 different acrylic intraocular lenses: Acrysof® Single-Piece IOL and Acrysof® WF, through evaluation of contrast sensitivity, glare testing, visual outcomes, wavefront, corneal topography, and patient satisfaction.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Acrysof single piece (SA60AT) | |
| DEVICE | Acrysof IQ (SN60WF) |
Timeline
- Start date
- 2004-07-01
- Completion
- 2005-05-01
- First posted
- 2006-08-21
- Last updated
- 2006-08-21
Source: ClinicalTrials.gov record NCT00366496. Inclusion in this directory is not an endorsement.