AcrySof Toric Clinical Results

Alcon Research144 enrolled

Overview

This study is an evaluation of visual outcomes of subjects implanted with the AcrySof Toric Intraocular Lenses (IOLs) Models SN60T3, SN60T4, and SN60T5.

Study Type

OBSERVATIONAL

Enrollment

144

Conditions

Cataracts Astigmatism

Interventions

T3DEVICE

Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T3

T4DEVICE

Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T4

T5DEVICE

Implantation of the AcrySof Toric Intraocular Lens (IOL) Model SN60T5

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Diagnosed with cataracts; has astigmatism falling in range of AcrySof Toric lens as assessed by the AcrySof Toric calculator Exclusion Criteria: * Ocular comorbidities affecting visual outcome data, * Prior refractive surgery, * Irregular astigmatism

Locations (1)

Alcon Call Center for Trial Locations

Fort Worth, Texas, United States

Outcomes

Primary Outcomes

Visual Acuity

Time frame: 1 day to 6 months

Secondary Outcomes

Postoperative refractive cylinder

Time frame: 1day to 6 months

Data from ClinicalTrials.gov

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