Evaluate the Ability of Systane Ultra to Improve Subjective Symptoms of Ocular Irritation Post 60 Min. Athletic Performance.

Alcon Research16 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Dry Eye Symptoms Visual Performance

Interventions

Systane® UltraOTHER

Polyethylene Glycol 400 0.4% / Propylene Glycol 0.3%

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Player/ Coach must answer "Yes" to the survey eligibility question. * Player/Coach must voluntarily agree to participate in survey Exclusion Criteria: * None.

Outcomes

Primary Outcomes

Effectiveness of eye drop basd on athlete's opinion/experience during a one hour practice session

Time frame: 60 minutes post-dosing with test article

Data from ClinicalTrials.gov

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