An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusis (LASIK) Therapy
NCT ID: NCT01854905
Last Updated: 2014-03-14
Study Results
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View full resultsBasic Information
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COMPLETED
400 participants
OBSERVATIONAL
2013-05-31
2013-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Patients Attending Consultation for LASIK
Patients attending consultation for LASIK on Day 1. No intervention or treatment is administered during the study.
No Treatment
Patients attending consultation for LASIK on Day 1. No intervention or treatment is administered during the study.
Interventions
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No Treatment
Patients attending consultation for LASIK on Day 1. No intervention or treatment is administered during the study.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Allergan
INDUSTRY
Responsible Party
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Principal Investigators
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Medical Director
Role: STUDY_DIRECTOR
Allergan
Locations
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Moscow, , Russia
Countries
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Other Identifiers
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MAF-AGN-OPH-DE-015
Identifier Type: -
Identifier Source: org_study_id
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