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Quantification of Posterior Capsule Opacification in Pediatric Cataract

NCT02968290 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2018-01-09

No results posted yet for this study

Summary

The purpose of this study is to quantify the opacity of posterior capsule in pediatric cataract comparing two intraocular lens materials.

Conditions

  • Posterior Capsule Opacification

Interventions

PROCEDURE

Cataract Surgery

Implant of intraocular lens hydrophobic or Implant of intraocular lens hydrophilic (Device)

DEVICE

Alcon AcrySof SA60AT

Implant of intraocular lens hydrophobic

DEVICE

Bausch Lomb AkreosA

Implant of intraocular lens hydrophilic

Sponsors & Collaborators

  • University of Sao Paulo

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
5 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-01
Primary Completion
2017-05-30
Completion
2017-11-30

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 NCT02968290 on ClinicalTrials.gov