Trials / Completed
CompletedNCT00758550
Visual Function After Bilateral Implantation of AcrySof® Toric
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 40 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study was to evaluate visual function of AcrySof Toric and AcrySof Natural Intraocular Lenses (IOLs) following implant for replacement of cataract.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | AcrySof® Toric IOL | AcrySof® Toric Intraocular Lens (IOL) implanted into the study eye following cataract extraction surgery |
| DEVICE | AcrySof Natural | AcrySof Natural Intraocular Lens (IOL) implanted into the study eye following cataract extraction surgery |
Timeline
- Start date
- 2007-04-01
- Primary completion
- 2008-06-01
- First posted
- 2008-09-25
- Last updated
- 2010-03-16
- Results posted
- 2010-03-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00758550. Inclusion in this directory is not an endorsement.