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
50 participants
OBSERVATIONAL
2008-12-31
2009-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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1
Measurement device
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Proof of eye exam within the last 3 months
* Corneal astigmatism of \<1.0 diopter
Exclusion Criteria
* Corneal trauma/disease
* Intraocular surgery
50 Years
ALL
Yes
Sponsors
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Alcon Research
INDUSTRY
Responsible Party
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Locations
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Alcon Call Center for Trial Locations
Fort Worth, Texas, United States
Countries
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Other Identifiers
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P-08-04
Identifier Type: -
Identifier Source: org_study_id
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