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Assessing the Performance of Lotrafilcon A Lenses During a Three Month Period

NCT00933166 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 169

Last updated 2012-07-10

Study results available
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Summary

The purpose of this trial is to assess the performance of an investigational contact lens over a three month period.

Conditions

  • Myopia

Interventions

DEVICE

Lotrafilcon A contact lens

Investigational silicone hydrogel, single vision, soft contact lens worn on a daily wear basis, flexible wear basis, or extended wear basis for three months

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2009-11-30
Completion
2009-11-30

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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 NCT00933166 on ClinicalTrials.gov