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A Study to Evaluate a New Silicone Hydrogel Contact Lens

NCT01309893 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2014-11-24

Study results available
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Summary

The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

Investigational Lens

Lenses worn on a daily wear basis for one week

DEVICE

Air Optix Aqua lens

Lenses worn on a daily wear basis for one week

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Robert Steffen, OD, MS · Bausch & Lomb Incorporated

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-12-31
Primary Completion
2011-01-31
Completion
2011-02-28

Countries

  • United States

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 NCT01309893 on ClinicalTrials.gov