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Comparative Study of the Wearing Satisfaction of Two Soft Contact Lens Designs.

NCT00768885 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2013-03-18

No results posted yet for this study

Summary

To evaluate the wearing satisfaction of a new design of the PureVision soft contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

PureVision 1

Currently marketed PureVision soft contact lens.

DEVICE

PureVision 2

Alternate design soft contact lens.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-09-30
Primary Completion
2008-10-31
Completion
2009-01-31

Countries

  • Japan

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 NCT00768885 on ClinicalTrials.gov