Trials / Completed
CompletedNCT00710931
Visual Function With Bilateral AcrySof® ReSTOR® Aspheric SN6AD1
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 35 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to prospectively evaluate the visual parameters in a series of patients after phacoemulsification cataract surgery in a series of patients bilaterally implanted with the AcrySof® ReSTOR® Aspheric +3.0 Intraocular Lens (IOL).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | AcrySof ReSTOR Aspheric IOL model SN6AD1 | Bilateral implantation of the AcrySof ReSTOR +3 Intraocular Lens (IOL) following cataract removal. |
Timeline
- Start date
- 2008-10-01
- Primary completion
- 2010-09-01
- Completion
- 2010-09-01
- First posted
- 2008-07-08
- Last updated
- 2011-12-12
- Results posted
- 2011-11-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00710931. Inclusion in this directory is not an endorsement.