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Product Feasibility of a New Silicone Hydrogel Contact Lens

NCT01309100 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 144

Last updated 2014-04-29

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 lens.

Conditions

  • Myopia

Interventions

DEVICE

Investigational Lens

Bausch \& Lomb investigational silicone hydrogel lens on a daily wear basis for 1 week.

DEVICE

Acuvue Oasys Lens

Johnson \& Johnson Acuvue Oasys contact lens on a daily wear basis for 1 week.

DEVICE

Air Optix Aqua Lens

Ciba Vision Air Optix Aqua contact lens on a daily wear basis for 1 week.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Tara Vaz, OD · Bausch & Lomb Incorporated

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2010-12-31
Completion
2011-01-31

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 NCT01309100 on ClinicalTrials.gov