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Visual Outcomes After Implantation of a New Multifocal Intraocular Lens

NCT01505816 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2012-01-09

No results posted yet for this study

Summary

This prospective nonrandomized study comprised patients with cataract, corneal astigmatism, and motivation for spectacle independence. In all cases, a Rayner M-flex® T toric Intraocular Lens will be implanted in the capsular bag. Three months postoperatively, distance, intermediate, and near visual acuities; spherical equivalent; residual refractive astigmatism; defocus curve; and contrast sensitivity will be evaluated. A patient-satisfaction and visual phenomena questionnaire will also be administered.

Conditions

  • Cataract

Interventions

DEVICE

Multifocal Intraocular Lens (RAYNER M-FLEX T TORIC IOL)

Multifocal IOL implantation

Sponsors & Collaborators

  • University of Sao Paulo

    collaborator OTHER

  • Hospital Oftalmologico de Brasilia

    lead OTHER

Principal Investigators

  • PATRICK F TZELIKIS, MD, PhD · HOSPITAL OFTALMOLOGICO BRASILIA

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
55 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2011-11-30
Completion
2012-01-31

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01505816 on ClinicalTrials.gov