A Study to Determine the Prevalence of Inflammatory Dry Eye Disease in Patients Prior to Cataract Removal
NCT ID: NCT01882413
Last Updated: 2015-12-03
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
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COMPLETED
204 participants
OBSERVATIONAL
2013-06-30
2014-03-31
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 with Planned Cataract Removal
Patients with planned cataract removal surgery are evaluated for the presence of inflammatory dry eye disease. No treatment is administered.
No intervention
No intervention
Interventions
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No intervention
No intervention
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Serious ocular injury, intraocular surgery, or refractive surgery within 6 months in the study eye
* Use of a contact lens within 4 weeks
50 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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Brandon, Manitoba, Canada
Halifax, Nova Scotia, Canada
Barrie, Ontario, Canada
Ottawa, Ontario, Canada
Toronto, Ontario, Canada
Boisbriand, Quebec, Canada
Countries
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Other Identifiers
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GMA-RES-012-001
Identifier Type: -
Identifier Source: org_study_id