Trials / Completed
CompletedNCT00818116
Visual Function Evaluation of Bilateral AcrySof ReSTOR Aspheric IOL
Visual Function After Implantation of Bilateral AcrySof ReSTOR Aspheric Intraocular Lens (IOL): Postmarket Evaluation
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 34 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 50 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate postoperative visual function in patients implanted bilaterally with the ReSTOR Aspheric Intraocular Lens (IOL).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | AcrySof ReSTOR Aspheric IOL | Bilateral implantation with the AcrySof ReSTOR Aspheric Intraocular Lens (IOL) for the replacement of cataract in the natural lens of the eye. |
Timeline
- Start date
- 2008-12-01
- Primary completion
- 2009-07-01
- First posted
- 2009-01-07
- Last updated
- 2010-07-30
- Results posted
- 2010-07-30
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00818116. Inclusion in this directory is not an endorsement.