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Feasibility of a New Silicone Hydrogel Lens

NCT01131130 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2014-04-30

Study results available
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Summary

The objective of this study is to determine the product feasibility of the investigational contact lens (Test) when compared to the currently marketed Acuvue Oasys contact lens (Control) and the Air Optix Aqua contact lens (Control) when worn by adapted wearers of soft contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

Investigational contact lens

After one week of wearing the first lens type, the participants will crossover to the second lens type for one week, and then crossover to the third lens type.

DEVICE

Acuvue Oasys Contact Lens

After one week of wearing the first lens type, the participants will crossover to the second lens type for one week, and then crossover to the third lens type.

DEVICE

Air Optix Aqua

After one week of wearing the first lens type, the participants will crossover to the second lens type for one week, and then crossover to the third lens type.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Gerard Carains, MCOptom, PhD · Bausch & Lomb Incorporated

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2010-06-30
Completion
2010-06-30

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 NCT01131130 on ClinicalTrials.gov