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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COMPLETED
144 participants
OBSERVATIONAL
2007-08-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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T3
Model SN60T3 assigned by AcrySof Toric calculator
T3
Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T3
T4
Model SN60T4 assigned by AcrySof Toric calculator
T4
Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T4
T5
Model SN60T5 assigned by AcrySof Toric calculator
T5
Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T5
Interventions
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T3
Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T3
T4
Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T4
T5
Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T5
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Prior refractive surgery,
* Irregular astigmatism
18 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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References
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Holladay JT, Wilcox RR, Koch DD, Wang L. Astigmatism analysis and reporting of surgically induced astigmatism and prediction error. J Cataract Refract Surg. 2022 Jul 1;48(7):799-812. doi: 10.1097/j.jcrs.0000000000000871.
Other Identifiers
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M07-007
Identifier Type: -
Identifier Source: org_study_id