Effect of Brimonidine Tartrate Ophthalmic Solution 0.15% on Pupil Diameter in Normal Eyes
NCT ID: NCT00413751
Last Updated: 2006-12-20
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
20 participants
OBSERVATIONAL
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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PROSPECTIVE
Interventions
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Brimonidine tartrate ophthalmic solution 0.15% (Alphagan P)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Females that are pregnant or lactating (non pregnant females of childbearing potential will have pregnancy test prior to participating in study)
* History of serious ocular, neurological, cardiovascular disease
* History of severe systemic disease
* History of arrhythmias or high blood pressure
* Patients currently taking any type of ocular or systemic medications except multivitamins.
* Patients with abnormal pupil shape, Addie's pupil, anisocoria, or abnormal pupil defect.
18 Years
50 Years
ALL
Yes
Sponsors
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Walter Reed Army Medical Center
FED
Principal Investigators
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KRAIG S. BOWER, MD
Role: PRINCIPAL_INVESTIGATOR
Walter Reed Army Medical Center
Locations
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Walter Reed Army Medical Center
Washington D.C., District of Columbia, United States
Countries
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Other Identifiers
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WRAMC WU #03-23004
Identifier Type: -
Identifier Source: org_study_id