Visual Outcomes of Subjects Bilaterally Implanted With ReSTOR Aspheric +4 vs. Tecnis or Acri.LISA

Alcon

Status and phase: Completed; Phase 4

Conditions: Cataract

Treatments: Device: ReSTOR; Device: Acri.LISA; Device: Tecnis

Study type: Interventional

Funder types: Industry

Identifiers

NCT00721253

M07-002

Details and patient eligibility

About

This is a study to compare visual outcomes of subjects bilaterally implanted w/ReSTOR to subjects bilaterally implanted with the Tecnis Multifocal Intraocular Lens (IOL) or Acri.LISA IOL

Enrollment: 42 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Diagnosed with cataracts

Exclusion criteria

• Preexisting condition likely to confound results; 1 D astigmatism by preoperative K-readings

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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42 participants in 3 patient groups

ReSTOR Aspheric +4

Active Comparator group

Description:

ACRYSOF ReSTOR Aspheric +4 Model SN6AD3

Treatment:

Device: ReSTOR

Tecnis MF

Active Comparator group

Description:

Abbott Medical Optics Tecnis Multifocal Intraocular Lens (IOL) Model ZM900

Treatment:

Device: Tecnis

Acri.LISA

Active Comparator group

Description:

Meditec Acri.LISA Intraocular Lens (IOL) Model 366D

Treatment:

Device: Acri.LISA