An Open-Label Study of an Ophthalmic Solution to Reduce Intraocular Pressure in Patients With Ocular Hypertension
NCT ID: NCT00825396
Last Updated: 2009-06-11
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
NA
12 participants
INTERVENTIONAL
2007-04-30
2009-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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C-KAD Ophthalmic Solution
C-KAD Ophthalmic Solution
4 drops applied daily for 150 days
Interventions
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C-KAD Ophthalmic Solution
4 drops applied daily for 150 days
Eligibility Criteria
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Inclusion Criteria
* Both eyes having best corrected visual acuity better than 20/50
Exclusion Criteria
* Closed or barely open anterior chamber or history of angle closure
50 Years
90 Years
ALL
No
Sponsors
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Chakshu Research, Inc.
INDUSTRY
Responsible Party
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Chakshu Research, Inc.
Principal Investigators
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Ira Wong, MD
Role: STUDY_DIRECTOR
Chakshu Research, Inc.
Locations
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Charlotte Eye, Ear, Nose & Throat Associates
Charlotte, North Carolina, United States
Countries
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Other Identifiers
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PCK-0106
Identifier Type: -
Identifier Source: org_study_id
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