Expired Study
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Santa Ana, California 92705


Purpose:

An investigational multi-purpose solution (MPS)was clinically evaluated against Biotrue MPS at specific time points over the course of four days. The study was conducted with PureVision lenses.


Criteria:

Inclusion Criteria: - were at least 18 years old; - were experienced contact lens wearers; - were correctable to at least 20/40 or better in both eyes with contact lenses; - were in good general health, with healthy eyes (other than requiring vision correction); - had not worn lenses for at least 12 hours before each baseline visit; - had a corneal staining score no greater than Grade 1 in either eye at time of enrollment; - had previously used an MPS or hydrogen peroxide solution successfully. Exclusion Criteria: - had a confirmed diagnosis of Sjögren's syndrome or other condition that results in a chronic and/or pathologic dry eye condition; - required concurrent ocular medication or have used ocular medication within 24 hours of entering the study; - had a known sensitivity or intolerance to any MPS, study products or ingredient(s); - were currently participating in any other clinical study; - had a condition or are in a situation that, in the investigator's opinion, may put them at significant risk, confound the study results, or interfere significantly with their participation in the study.


NCT ID:

NCT01240122


Primary Contact:

Principal Investigator
Eugenia Y Kao, OD
AMO


Backup Contact:

N/A


Location Contact:

Santa Ana, California 92705
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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