Bioequivalency Study of 100 mg Cilostazol Tablets Under Fasting Conditions
NCT ID: NCT00602173
Last Updated: 2018-01-23
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
32 participants
INTERVENTIONAL
2003-05-31
2003-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Interventions
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Cilostazol
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Treatment with known enzyme altering drugs.
* History of allergic or adverse response to Cilostazol or any comparable or similar product.
18 Years
45 Years
ALL
Yes
Sponsors
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Roxane Laboratories
INDUSTRY
Responsible Party
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Roxane Labortories, Inc.
Principal Investigators
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Daniel V Freeland, DO
Role: PRINCIPAL_INVESTIGATOR
CEDRA Clinical Research, LLC
Locations
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CEDRA Clinical Research, LLC
Austin, Texas, United States
Countries
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Other Identifiers
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CILO-03
Identifier Type: -
Identifier Source: org_study_id
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