Relationship Between Topiramate Use and Ocular Angle Status
NCT ID: NCT00153699
Last Updated: 2007-10-31
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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UNKNOWN
PHASE4
15 participants
INTERVENTIONAL
2004-09-30
2007-07-31
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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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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Topiramate
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Recent exposure to topiramate (\<3 months).
* Moderate to severe renal failure.
* Known history of renal calculi or hepatic failure
* Inability to give informed consent.
* Pregnant women or women of child-bearing age who do not practise an acceptable means of contraception.
* Patients known to have angle-closure glaucoma.
18 Years
75 Years
ALL
No
Sponsors
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Hong Kong Eye Hospital
OTHER
Chinese University of Hong Kong
OTHER
Principal Investigators
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Dexter YL Leung, MRCS
Role: PRINCIPAL_INVESTIGATOR
Hong Kong Eye Hospital
Howan Leung, MRCP
Role: PRINCIPAL_INVESTIGATOR
Chinese University of Hong Kong
Locations
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Hong Kong Eye Hospital
Kowloon, , Hong Kong
Prince of Wales Hospital
Shatin, , Hong Kong
Countries
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Other Identifiers
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CRE-2004.310
Identifier Type: -
Identifier Source: org_study_id
NCT00518063
Identifier Type: -
Identifier Source: nct_alias