Evaluation of Comfort in Symptomatic Contact Lens Wearers
NCT ID: NCT04963543
Last Updated: 2021-11-03
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
NA
17 participants
INTERVENTIONAL
2021-07-22
2021-10-29
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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FID123238
FID123238 applied to the ocular surface, 1 application per day, for five consecutive days
FID123238
Lubricant applied to the ocular surface
Interventions
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FID123238
Lubricant applied to the ocular surface
Eligibility Criteria
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Inclusion Criteria
* Habitually wears daily disposable soft contact lenses in both eyes;
* Is able to achieve 20/40 or better monocular VA with habitual contact lenses;
* Has a pair of spectacles for vision correction.
Exclusion Criteria
* Has any known active ocular disease and/or infection;
* Is pregnant or lactating;
18 Years
ALL
No
Sponsors
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Alcon Research
INDUSTRY
Responsible Party
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Principal Investigators
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Clinical Trial Lead, Dry Eye
Role: STUDY_DIRECTOR
Alcon Research, LLC
Locations
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Alcon Investigative Site 6189
Waterloo, Ontario, Canada
Countries
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Other Identifiers
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DEJ475-E003
Identifier Type: -
Identifier Source: org_study_id