Trials / Terminated
TerminatedNCT00710905
Visual Function With Contralateral AcrySof® ReSTOR® Aspheric SN6AD1 and SN6AD3
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 50 (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 Intraocular Lens (IOL) Models SN6AD1 And SN6AD3.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | AcrySof ReSTOR Aspheric IOL models SN6AD1 and SN6AD3 | Contralateral implantation of AcrySof ReSTOR +3 Intraocular Lens (IOL) in one eye, AcrySof ReSTOR +4 IOL in the other eye following cataract removal. |
Timeline
- Start date
- 2009-10-01
- Primary completion
- 2010-09-01
- Completion
- 2010-09-01
- First posted
- 2008-07-08
- Last updated
- 2011-11-24
- Results posted
- 2011-11-08
Locations
2 sites across 1 country: Canada
Source: ClinicalTrials.gov record NCT00710905. Inclusion in this directory is not an endorsement.