Status:
COMPLETED
Clinical Evaluation of Opti-Free III (FID 109182) Compared to Opti-Free Plus® in Japan
Lead Sponsor:
Alcon Research
Conditions:
Corneal Staining
Eligibility:
All Genders
20+ years
Phase:
NA
Brief Summary
The purpose of this study is to compare an investigational contact lens care product (FID 109182) to a commercially available contact lens product (Opti-Free Plus®) for corneal staining when used with...
Eligibility Criteria
Inclusion
- Soft contact lenses habitual wearer, both eyes.
- Voluntarily sign Informed Consent.
- Other protocol-defined inclusion criteria may apply.
Exclusion
- Unable to tolerate the ingredients in Opti-Free® and similar contact lens care products.
- Potential use of eye drops during the study, including over-the-counter products, except for artificial tear eye drops.
- Eye infection, blepharitis, iris inflammation, or severe eye inflammation.
- Corneal staining greater than Grade 1 at baseline.
- Pregnant, lactating, or intend to become pregnant during study period.
- Other protocol-defined exclusion criteria may apply.
Key Trial Info
Start Date :
November 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2014
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT02251561
Start Date
November 1 2013
End Date
May 1 2014
Last Update
June 10 2015
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