Status:
COMPLETED
Evaluate the Ability of Systane Ultra to Improve Subjective Symptoms of Ocular Irritation Post 60 Min. Athletic Performance.
Lead Sponsor:
Alcon Research
Conditions:
Dry Eye Symptoms
Visual Performance
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The primary objective of this study is to compare visual degradation in a stressed (forced stare) environment in patients before and after acute administration of Systane Ultra.
Eligibility Criteria
Inclusion
- Player/ Coach must answer "Yes" to the survey eligibility question.
- Player/Coach must voluntarily agree to participate in survey
Exclusion
- None.
Key Trial Info
Start Date :
June 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT00938951
Start Date
June 1 2009
Last Update
February 9 2012
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