Trials / Completed
CompletedNCT01045733
A Comparison of Corneal Aberrations in Subjects With Contralateral AcrySof IQ Toric Intraocular Lens (IOL) and AcrySof IQ IOL With Limbal Relaxing Incision (LRI)
A Prospective Contralateral Comparison of Corneal Aberrations in Subjects Undergoing Aspheric Lens Implantation With Concomitant LRI and Aspheric Toric IOL Implantation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 70 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study was to evaluate and compare postoperative corneal aberrations and visual parameters in patients contralaterally implanted with an AcrySof IQ Toric intraocular lens (IOL) and AcrySof IQ Aspheric IOL with concomitant limbal relaxing incision.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | AcrySof IQ Toric IOL | AcrySof IQ Toric intraocular lens implanted in the capsular bag of the eye during cataract surgery. The IOL is intended for the lifetime of the patient. |
| DEVICE | AcrySof IQ Aspheric IOL | AcrySof IQ aspheric intraocular lens implanted in the capsular bag of the eye during cataract surgery. The IOL is intended for the lifetime of the patient. |
| PROCEDURE | Limbal Relaxing Incision (LRI) | An incision was made at the corneal-limbal junction during cataract surgery for the purpose of relaxing corneal curvature, ie., correcting astigmatism. |
Timeline
- Start date
- 2009-12-01
- Primary completion
- 2011-05-01
- Completion
- 2011-05-01
- First posted
- 2010-01-11
- Last updated
- 2012-11-29
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01045733. Inclusion in this directory is not an endorsement.