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Evaluation of the Performance of Non-molded Soft Contact Lenses

NCT00371787 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 38

Last updated 2011-01-10

Study results available
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Summary

To evaluate the performance of the study soft lens for vision, comfort, physiology and lens surface properties.

Conditions

  • Ametropia

Interventions

DEVICE

Soft contact lens

Soft contact lens

Sponsors & Collaborators

  • CIBA VISION

    collaborator INDUSTRY

  • University of Waterloo

    lead OTHER

Principal Investigators

  • Desmond Fonn · Centre for Contact Lens Research

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-08-31
Primary Completion
2007-12-31
Completion
2007-12-31

Countries

  • Canada

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 NCT00371787 on ClinicalTrials.gov