Phase 4 Study Comparing IOP Lowering in OAG or OH in Caucasian or Japanese Subjects C-02-32
NCT ID: NCT00047606
Last Updated: 2012-08-17
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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TERMINATED
PHASE4
84 participants
INTERVENTIONAL
2002-08-31
2003-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
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IOP Lowering Medications
Eligibility Criteria
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Inclusion Criteria
18 Years
ALL
No
Sponsors
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Alcon Research
INDUSTRY
Responsible Party
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Other Identifiers
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C-02-32
Identifier Type: -
Identifier Source: secondary_id
C-02-32
Identifier Type: -
Identifier Source: org_study_id
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