Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus Limbal Relaxing Incision (LRI) Patients
NCT ID: NCT00929747
Last Updated: 2012-04-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
PHASE4
INTERVENTIONAL
2009-06-30
2009-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Toric IOL
AcrySof IQ Toric IOL
Toric
Unilateral implantation of the AcrySof IQ Toric IOL
Limbal Relaxing Incision
AcrySof IQ with Limbal Relaxing Incision
Limbal Relaxing Incision
Unilateral implantation of a AcrySof IQ (SN60WF) IOL with concomitant LRI at the time of surgery
Interventions
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Toric
Unilateral implantation of the AcrySof IQ Toric IOL
Limbal Relaxing Incision
Unilateral implantation of a AcrySof IQ (SN60WF) IOL with concomitant LRI at the time of surgery
Eligibility Criteria
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Inclusion Criteria
2. good ocular health
3. 0.5 D to 2.0 D of corneal astigmatism
Exclusion Criteria
2. irregular astigmatism
3. prior or ongoing corneal disease or scarring
4. history of ocular disease
18 Years
70 Years
ALL
No
Sponsors
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Alcon Research
INDUSTRY
Responsible Party
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Locations
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Alcon Call Center for Trial Locations
Fort Worth, Texas, United States
Countries
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Other Identifiers
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M08-008
Identifier Type: -
Identifier Source: org_study_id
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