MedPath

Low Cylinder Toric

Phase 4
Completed
Conditions
Cataracts
Interventions
Device: Toric IOL (SN60T3)
Registration Number
NCT00732030
Lead Sponsor
Alcon Research
Brief Summary

Study evaluates the visual outcomes and patient satisfaction after implantation of a toric intraocular lens (IOL).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
26
Inclusion Criteria
  • Diagnosed with Cataracts
  • Predicted residual corneal astigmatism between 0.75 and 1.03 Diopters (D)
Exclusion Criteria
  • Preoperative ocular pathology
  • Planned monovision

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
AcrySof Toric T3Toric IOL (SN60T3)Each enrolled eye receives AcrySof Toric Model SN60T3 Intraocular Lens (IOL)
Primary Outcome Measures
NameTimeMethod
Uncorrected Distance Visual Acuity6 months

Uncorrected Distance Visual Acuity at month 6 measured in logMAR. LogMAR is the "logarithm of the minimum angle of resolution". It is a unit of measure for visual acuity (VA).

Best Corrected Distance Visual Acuity6 Months

Best Corrected Distance Visual Acuity at month 6 measured in LogMAR. LogMAR is the "logarithm of the minimum angle of resolution". It is a unit of measure for visual acuity (VA).

Residual Refractive Cylinder6 Month

Residual Refractive Cylinder at month 6 measured in diopters (D).

Secondary Outcome Measures
NameTimeMethod
Patient Satisfaction Survey6 months

Satisfaction for daytime distance vision, nighttime distance vision, and indoors distance vision on a scale of 1 to 5, with 1 being very dissatisfied and 5 being very satisfied.

Trial Locations

Locations (1)

Alcon Call Center for Trial Locations

🇺🇸

Fort Worth, Texas, United States

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