Trials / Withdrawn
WithdrawnNCT00929747
Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus Limbal Relaxing Incision (LRI) Patients
Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus LRI Patients
- Status
- Withdrawn
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
A prospective evaluation of postoperative corneal aberrations and visual parameters in patients assigned to either an AcrySof IQ Toric intraocular lens (IOL) group or a group implanted with a SN60WF IOL and having concomitant limbal relaxing incision.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Toric | Unilateral implantation of the AcrySof IQ Toric IOL |
| PROCEDURE | Limbal Relaxing Incision | Unilateral implantation of a AcrySof IQ (SN60WF) IOL with concomitant LRI at the time of surgery |
Timeline
- Start date
- 2009-06-01
- Primary completion
- 2009-10-01
- Completion
- 2009-10-01
- First posted
- 2009-06-29
- Last updated
- 2012-04-12
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00929747. Inclusion in this directory is not an endorsement.