Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
INTERVENTIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SINGLE
Interventions
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Optive, Systane
Eligibility Criteria
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Inclusion Criteria
* Mild to moderate dry eye symptoms
* Score of at least 2 and no more than 4 on the SESOD at the initial screening visit
* Likely to complete all study visits and able to provide informed consent
Exclusion Criteria
* Known contraindications to any study medication or ingredients
* Active ocular diseases or uncontrolled systemic disease (blepharitis patients that are actively being treated or disease that is uncontrollable)
* Ocular surgery within the past 3 months,
* Active ocular allergies
18 Years
ALL
No
Sponsors
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Innovative Medical
INDUSTRY
Principal Investigators
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Milton Hom, OD
Role: PRINCIPAL_INVESTIGATOR
Private Practice
Locations
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Private Practice
Azusa, California, United States
Countries
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Other Identifiers
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5283
Identifier Type: -
Identifier Source: org_study_id