AcrySof Toric Clinical Results

Clinical Results With the AcrySof Toric Intraocular Lens (IOL)

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01214863

Enrollment

144

Registered

2010-10-05

Start date

2007-08-31

Completion date

Unknown

Last updated

2012-10-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Astigmatism, Cataracts

Keywords

Toric Intraocular Lens (IOL)

Brief summary

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

Interventions

DEVICET3

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

DEVICET4

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

DEVICET5

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

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Visual Acuity	1 day to 6 months

Secondary

Measure	Time frame
Postoperative refractive cylinder	1day to 6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026