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Last Updated: November 24, 2024

CLINICAL TRIALS PROFILE FOR IBUPROFEN SODIUM


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All Clinical Trials for IBUPROFEN SODIUM

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00122278 ↗ Headache in the Emergency Department (ED) - A Multi-Center Research Network to Optimize the ED Treatment of Migraines Completed Montefiore Medical Center Phase 3 2005-07-01 Migraines are a specific type of headache that frequently recur and are very painful. Although there are many medications that are effective against migraines, none of these medications cure 100% of migraines. Another problem with migraines is that although many times they get better after intravenous (IV) treatment in the emergency room (ER), about 1/3 of the time migraines recur the next day. The purpose of this research project is to see if adding a medication called dexamethasone to standard ER therapy will help patients get better quicker and stay pain-free more often than if they receive placebo.
NCT00261586 ↗ A Safety Trial to Compare Different Analgesics in Combination With Low Dose Aspirin to Study Their Bleeding Properties and Their Effects on the Stomach Completed Johnson & Johnson Consumer and Personal Products Worldwide Phase 4 1969-12-31 The purpose of this study is to compare several analgesics given in approved daily doses in combination with a daily cardioprotective dose of aspirin (81 mg), to study their bleeding properties and their effects on the stomach in healthy volunteers.
NCT00264381 ↗ Management of Superficial Thrombophlebitis Completed Pfizer Phase 4 2002-10-01 The purpose of this study is to test the hypothesis that Fragmin (dalteparin sodium) subcutaneously once daily for 7 days is more effective than Ibuprofen given orally three times daily for 7 days for the treatment of superficial thrombophlebitis (STP).
NCT00264381 ↗ Management of Superficial Thrombophlebitis Completed University of Oklahoma Phase 4 2002-10-01 The purpose of this study is to test the hypothesis that Fragmin (dalteparin sodium) subcutaneously once daily for 7 days is more effective than Ibuprofen given orally three times daily for 7 days for the treatment of superficial thrombophlebitis (STP).
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for IBUPROFEN SODIUM

Condition Name

Condition Name for IBUPROFEN SODIUM
Intervention Trials
Pain 2
Sprains and Strains 2
Pain, Postoperative 2
Acute Pain 2
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Condition MeSH

Condition MeSH for IBUPROFEN SODIUM
Intervention Trials
Pain, Postoperative 5
Migraine Disorders 4
Pulpitis 2
Emergencies 2
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Clinical Trial Locations for IBUPROFEN SODIUM

Trials by Country

Trials by Country for IBUPROFEN SODIUM
Location Trials
United States 21
Brazil 2
Canada 2
France 2
Jordan 1
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Trials by US State

Trials by US State for IBUPROFEN SODIUM
Location Trials
California 4
Utah 3
Pennsylvania 3
Illinois 2
Oklahoma 2
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Clinical Trial Progress for IBUPROFEN SODIUM

Clinical Trial Phase

Clinical Trial Phase for IBUPROFEN SODIUM
Clinical Trial Phase Trials
Phase 4 13
Phase 3 6
Phase 2/Phase 3 2
[disabled in preview] 3
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Clinical Trial Status

Clinical Trial Status for IBUPROFEN SODIUM
Clinical Trial Phase Trials
Completed 21
Recruiting 5
Not yet recruiting 4
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Clinical Trial Sponsors for IBUPROFEN SODIUM

Sponsor Name

Sponsor Name for IBUPROFEN SODIUM
Sponsor Trials
Pfizer 3
Cairo University 3
Bayer 2
[disabled in preview] 2
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Sponsor Type

Sponsor Type for IBUPROFEN SODIUM
Sponsor Trials
Other 46
Industry 14
NIH 2
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