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
40 participants
INTERVENTIONAL
2004-05-31
2006-08-31
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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Naproxen
Eligibility Criteria
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Inclusion Criteria
2. No history of allergy or adverse reaction to any NSAID
3. No use of any NSAID in past 2 weeks
4. No history of peptic ulcer disease (PUD), gastroesophageal disease (GERD), or gastritis
5. No major medical history including but not limited to diabetes, hypertension, asthma, kidney disease and coronary artery disease
6. Currently not taking any medication including oral contraceptives
Exclusion Criteria
2. History of allergy or adverse reaction to any NSAID
3. Use of any NSAID in past 2 weeks
4. History of a bleeding disorder
5. History of PUD, GERD, or gastritis
6. Pregnant
7. A medical history of diabetes, hypertension, asthma, kidney disease or coronary artery disease
8. Taking any medication including oral contraceptives
18 Years
30 Years
ALL
Yes
Sponsors
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University of Oklahoma
OTHER
Principal Investigators
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LaMont Cavanagh, MD
Role: PRINCIPAL_INVESTIGATOR
University of Oklahoma-Tulsa
Locations
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Family Practice - CMT
Tulsa, Oklahoma, United States
Countries
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Other Identifiers
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11186
Identifier Type: -
Identifier Source: org_study_id