MedTrace Logo

Clinical Outcomes After Bilateral Implantation of ZEISS AT LISA TRI AND TRI TORIC IOL

NCT02770924 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2017-09-14

No results posted yet for this study

Summary

The aim of this study is to evaluate the visual function of patients with bilateral implantation of the IOL trifocal ZEISS AT LISA TRI AND TRI TORIC by means of visual acuity tests with and without optical correction, sensitivity curve contrast, defocus curve and quality questionnaire visual function (VFQ-25).

Conditions

  • Cataract

Interventions

DEVICE

AT LISA TRI TORIC

phacoemulsification with IOL implantation

DEVICE

AT LISA TRI

phacoemulsification with IOL implantation

Sponsors & Collaborators

  • Instituto Paulista de Estudos e Pesquisa em Oftalmologia

    collaborator OTHER

  • Eye Clinic Day Hospital, São Paulo

    collaborator OTHER

  • Federal University of São Paulo

    lead OTHER

Principal Investigators

  • Rubens Belfort, MD, PhD · IPEPO Instituto Paulista de Estudos e Pesquisas em Oftalmologia

Study Design

Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2017-07-31
Completion
2017-09-13

Countries

  • Brazil

Study Locations

More Related Trials

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 NCT02770924 on ClinicalTrials.gov