Trials / Completed
CompletedNCT00963560
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
- 132 (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 Presbyopia-Correcting Intraocular Lenses (IOLs).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ReSTOR +3 | Bilateral implantation of the AcrySof ReSTOR Aspheric +3 Model SN6AD1 Intraocular lens (IOL) for the treatment of cataract. |
| DEVICE | Crystalens HD | Bilateral implantation of the Crystalens HD intraocular lens (IOL) for the treatment of cataract. |
| DEVICE | Crystalens AO | Bilateral implantation of the Crystalens AO intraocular lens (IOL) for the treatment of cataract. |
Timeline
- Start date
- 2009-08-01
- Primary completion
- 2011-03-01
- First posted
- 2009-08-21
- Last updated
- 2011-08-09
- Results posted
- 2011-08-09
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00963560. Inclusion in this directory is not an endorsement.