Trials / Completed
CompletedNCT01166971
A Comparison of Visual Function After Bilateral Implantation of Presbyopia-correcting Intraocular Lenses (IOLs)
A Randomized, Subject-masked Comparison of Visual Function After Bilateral Implantation of Presbyopia-correcting IOLs
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 65 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to prospectively evaluate postoperative visual and refractive parameters in a series of subjects bilaterally implanted with the AcrySof® IQ ReSTOR® +3 versus those bilaterally implanted with the Tecnis Multifocal 1-piece.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ReSTOR +3 | Bilateral implantation of ReSTOR +3 Intraocular Lenses (IOLs) after cataract extraction |
| DEVICE | Tecnis MF | Bilateral implantation of Tecnis Multifocal (MF) Intraocular Lenses (IOLs) after cataract extraction |
Timeline
- Start date
- 2010-07-01
- Primary completion
- 2011-03-01
- First posted
- 2010-07-21
- Last updated
- 2011-11-24
- Results posted
- 2011-11-08
Locations
3 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01166971. Inclusion in this directory is not an endorsement.