- Trials with a EudraCT protocol (53)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (70)
53 result(s) found for: Naproxen.
Displaying page 1 of 3.
EudraCT Number: 2014-005305-20 | Sponsor Protocol Number: BAYH6689/15833 | Start Date*: 2015-02-09 |
Sponsor Name:Bayer HealthCare AG | ||
Full Title: A Pilot Self Selection Trial of an Extended-Release Over-the-Counter Analgesic | ||
Medical condition: Pain | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2005-005422-31 | Sponsor Protocol Number: COX189A2425 | Start Date*: 2006-05-05 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A 16-day, randomized, double-blind, double-dummy, placebo-controlled, parallel-group trial comparing lumiracoxib 100mg o.d. with naproxen 500 mg b.i.d. plus omeprazole 20mg o.d. and placebo in heal... | ||
Medical condition: Healthy volunteers. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005442-39 | Sponsor Protocol Number: Better Life in Osteoarthritis | Start Date*: 2006-10-24 |
Sponsor Name:Division of Rheumatology | ||
Full Title: Randomized controlled trial of prednisolone in the treatment of osteaoarthritis of the hand | ||
Medical condition: Osteoarthritis of the hands | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001354-95 | Sponsor Protocol Number: 149/11 | Start Date*: 2013-06-13 | |||||||||||
Sponsor Name:Keele University | |||||||||||||
Full Title: A randomised, multi-centre, open-label, active-comparator, pragmatic clinical trial of low-dose colchicine versus naproxen in patients with acute gout. | |||||||||||||
Medical condition: Acute Gout | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003737-26 | Sponsor Protocol Number: A3191342 | Start Date*: 2015-04-07 |
Sponsor Name:Pfizer Inc | ||
Full Title: A Phase 4, 6-week, randomized double-blind, multicenter, active-controlled trial to evaluate the effects of Celecoxib (Celebrex®) or Naproxen on blood pressure in paediatric subjects with juvenile ... | ||
Medical condition: Juvenile idiopathic arthritis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2010-024641-71 | Sponsor Protocol Number: 071(D)SC10102 | Start Date*: 2011-05-12 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: A randomized, multicenter, double-blind study assessing the efficacy and safety of two topical 10% naproxen gel formulations in the treatment of benign soft-tissue injuries. | |||||||||||||
Medical condition: Benign soft-tissue injuries. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001301-23 | Sponsor Protocol Number: APHP200387 | Start Date*: 2020-04-10 |
Sponsor Name:Assistance Publique - Hôpitaux de Paris | ||
Full Title: Efficacy of Addition of Naproxen in the Treatment of critically ill Patients Hospitalized for COVID-19 Infection / Enacovid Study | ||
Medical condition: COVID-19 Infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000415-25 | Sponsor Protocol Number: NAS-S-01 | Start Date*: 2013-11-07 | ||||||||||||||||
Sponsor Name:Clinirx Tangent Research | ||||||||||||||||||
Full Title: A randomized, double-blind, placebo controlled study to evaluate the efficacy and safety of Naproxen, Simvastatin and their combination, compared to placebo as add-on to anti-psychotics in the trea... | ||||||||||||||||||
Medical condition: schizophrenia and schizoaffective disorder. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: RO (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001586-18 | Sponsor Protocol Number: TD-04-01 | Start Date*: 2004-10-26 |
Sponsor Name:Wyeth Consumer Healthcare | ||
Full Title: A Safety Study of TDS-943 | ||
Medical condition: Of Product: Relieve pain and swelling in joints, muscles | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-005020-29 | Sponsor Protocol Number: R475-OA-1611 | Start Date*: 2018-04-10 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-blind, Multi-dose, Placebo and Naproxen-Controlled Study to Evaluate the Efficacy and Safety of Fasinumab in Patients with Pain Due to Osteoarthritis of the Knee or Hip | ||||||||||||||||||
Medical condition: Pain due to osteoarthritis of the knee or hip | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) LT (Completed) GB (GB - no longer in EU/EEA) DK (Completed) PL (Completed) HU (Completed) ES (Ongoing) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005268-13 | Sponsor Protocol Number: BAYH6689/13129 | Start Date*: 2015-02-05 |
Sponsor Name:Bayer HealthCare AG | ||
Full Title: An Open Label, Actual Use Study in Consumers Taking an Extended-Release Over the Counter NSAID in a Naturalistic Setting | ||
Medical condition: Pain | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2020-004343-92 | Sponsor Protocol Number: 21559 | Start Date*: 2021-06-23 |
Sponsor Name:Bayer Healthcare LLC. | ||
Full Title: Randomized, Controlled, Double-blind, Placebo-controlled, Multi-center Hypothesis-finding Trial to Compare the Efficacy and Safety of a 10% Naproxen Gel vs. a 2.32% Diclofenac Diethylamine Gel and ... | ||
Medical condition: acute strains, sprains or bruises of the lower extremities following blunt trauma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005272-28 | Sponsor Protocol Number: BAYH6689/15142 | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo Controlled Trial to Assess the Analgesic Efficacy and Safety of Extended Release Naproxen Sodium Tablets in Postsurgical Dental Pain | |||||||||||||
Medical condition: Pain, Postoperative | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005049-67 | Sponsor Protocol Number: 19762 | Start Date*: 2018-08-29 | |||||||||||
Sponsor Name:Bayer HealthCare LLC | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Trial to Compare the Duration of Analgesic Efficacy and Safety of Naproxen Sodium Tablets and Ibuprofen Tablets in Postsurgical Dental Pain | |||||||||||||
Medical condition: Pain relief | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005269-66 | Sponsor Protocol Number: BAYH6689/13130 | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Trial Assessing the Analgesic Efficacy of a Single, Oral Dose of an Extended Release Naproxen Sodium Tablet in Postsurgical Den... | |||||||||||||
Medical condition: Toothache | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020475-23 | Sponsor Protocol Number: B0041007 | Start Date*: 2010-10-05 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 2 RANDOMIZED, DOUBLE-BLINDED, DOUBLE-DUMMY, PLACEBO AND ACTIVE CONTROLLED TWO COHORT TWO-WAY CROSS-OVER, MULTI-CENTRE CLINICAL TRIAL TO EXAMINE THE PAIN RELIEF PRODUCED BY 2 WEEKS OF DAILY... | |||||||||||||
Medical condition: Chronic pain in patients with Osteo-arthritis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003513-33 | Sponsor Protocol Number: 21069 | Start Date*: 2020-05-20 | ||||||||||||||||
Sponsor Name:Bayer HealthCare LLC | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Single-Dose, Parallel, Placebo-Controlled Trial to Determine the Dose of Caffeine in a Fixed Dose Combination Tablet of Naproxen Sodium and Caffeine to Effectively Allev... | ||||||||||||||||||
Medical condition: Pain, Postoperative | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005316-41 | Sponsor Protocol Number: BAYH6689/15647 | Start Date*: 2015-02-09 |
Sponsor Name:Bayer HealthCare AG | ||
Full Title: An Actual Use Trial In A Simulated OTC Environment of an Extended-Release Over-the-Counter NSAID | ||
Medical condition: Pain | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2018-001020-19 | Sponsor Protocol Number: NL65360.18 | Start Date*: 2019-04-05 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Nifedipine induced pain relief during hysteroscopy | ||
Medical condition: Pain intensity during hysteroscopy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-000078-21 | Sponsor Protocol Number: HCT 3012-X-303 | Start Date*: 2007-10-11 | |||||||||||
Sponsor Name:NicOx S.A | |||||||||||||
Full Title: A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo bid and Naproxen 500 mg bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HC... | |||||||||||||
Medical condition: Osteoarthritis of the Hip | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) DE (Completed) BG (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
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