Performance Evaluation of DAILIES® TOTAL1™ in First Time Contact Lens Wearers
NCT ID: NCT01494545
Last Updated: 2013-07-19
Study Results
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View full resultsBasic Information
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COMPLETED
NA
102 participants
INTERVENTIONAL
2011-12-31
2012-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Delefilcon A
Delefilcon A contact lenses worn in both eyes on a daily wear, daily disposable basis for two weeks. A new pair was inserted each day.
Delefilcon A contact lens
Silicone hydrogel contact lens CE-marked for single use, daily disposable wear
Interventions
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Delefilcon A contact lens
Silicone hydrogel contact lens CE-marked for single use, daily disposable wear
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* No previous contact lens experience or attempt to try contact lenses (neophyte).
* Willing to wear study lenses for at least 8 hours a day for at least 5 days a week.
* Use spectacle lenses for vision correction.
Exclusion Criteria
* Prior wear experience with rigid or soft contact lenses.
* Systemic or ocular disease or disorder that would negatively affect the conduct or outcome of the study.
* History of ocular surgery/trauma within the last six months.
* Pregnant or nursing women.
* Participation in any other ophthalmic drug or device clinical trial within 30 days of enrollment.
18 Years
44 Years
ALL
No
Sponsors
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Alcon Research
INDUSTRY
Responsible Party
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Principal Investigators
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Jami Kern, PhD
Role: STUDY_DIRECTOR
Alcon Research
Other Identifiers
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P-347-C-016
Identifier Type: -
Identifier Source: org_study_id
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