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Evaluation of Two Silicone Hydrogel Lenses Over a One Month Period

NCT00810511 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 213

Last updated 2023-12-05

Study results available
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Summary

The purpose of this trial is to compare two different contact lenses during 4 weeks of wear.

Conditions

  • Myopia

Interventions

DEVICE

Lotrafilcon A contact lens

Silicone hydrogel contact lens

DEVICE

Comfilcon A contact lens

Silicone hydrogel contact lens

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2009-01-31
Completion
2009-01-31

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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 NCT00810511 on ClinicalTrials.gov