- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
25 result(s) found for: Etoricoxib.
Displaying page 1 of 2.
EudraCT Number: 2007-004274-10 | Sponsor Protocol Number: Etoric-TE-1 | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:Freistaat Bayern | |||||||||||||
Full Title: Analgesic efficacy and safety of etoricoxib in ear nose throat surgery | |||||||||||||
Medical condition: The aim of this study is to test the analgesic efficacy and safety of etoricoxib (90 mg or 120 mg qd. perioperatively) for post-operative pain relief in tonsillectomy patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004098-17 | Sponsor Protocol Number: 35195 | Start Date*: 2009-03-31 |
Sponsor Name:East Tallinn Central Hospital | ||
Full Title: Double-Blind, Randomized, Placebo -Controlled Study to Evaluate the Efficacy of Pre-operative Administration of Etoricoxib 120 mg, Etoricoxib 120 mg and Paracetamol 1 g Combination or Placebo in th... | ||
Medical condition: Pre-operative Administration of Etoricoxib 120 mg, Etoricoxib 120 mg and Paracetamol 1 g Combination or Placebo in the Treatment of Postoperative Pain in Patients Undergoing Gynaecologic Laparoscop... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: EE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003854-80 | Sponsor Protocol Number: 02B2005 | Start Date*: 2006-01-31 |
Sponsor Name:Department of Experimental and Clinical Pharmacology and Toxicology, Friedrich-Alexander-University | ||
Full Title: Modulation of the Surgical Inflammatory Response by Etoricoxib: Peripheral versus Central | ||
Medical condition: Patients with osteoarthritis undergoing elective primary single hip arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000487-27 | Sponsor Protocol Number: 0663-806 | Start Date*: 2004-08-10 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A Double-Blind, Parallel-Group, 4-week Trial to Assess the Efficacy and Safety of Etoricoxib 60mg and Diclofenac 150mg in Patients with Chronic Low Back Pain | |||||||||||||
Medical condition: Chronic Low Back Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004867-21 | Sponsor Protocol Number: 0663-097 | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: Ensayo multicéntrico doble ciego controlado con placebo para estudiar la eficacia y la tolerabilidad de MK-0663/etoricoxib en el tratamiento del dolor después de histerectomía abdominal A Double... | |||||||||||||
Medical condition: Histerectomía Abdominal Abdominal Hysterectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) EE (Completed) HU (Completed) IE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019872-65 | Sponsor Protocol Number: MK-0663-108 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III, Two-Part, Randomized, Double-Blind, Active Comparator-Controlled, Multicenter Clinical Trial to Study the Relative Efficacy and Tolerability of Two Doses of MK-0663/Etoricoxib in Patie... | |||||||||||||
Medical condition: Ankylosing Spondylitis (AS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) FI (Completed) BE (Completed) AT (Completed) GB (Completed) EE (Completed) SK (Completed) CZ (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019871-31 | Sponsor Protocol Number: MK-0663-107 | Start Date*: 2010-10-18 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III, Two-Part, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Clinical Trial to Assess the Relative Efficacy and Tolerability of Two Doses of MK- 0663/Etoricoxib in Patients wit... | |||||||||||||
Medical condition: Rheumatoid Arthritis (RA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) BE (Completed) AT (Completed) LT (Completed) GB (Completed) DE (Completed) SK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000395-32 | Sponsor Protocol Number: 2006001 | Start Date*: 2006-03-29 |
Sponsor Name:King's College London | ||
Full Title: The effect of COX-2 Inhibition on Reducing Central Sensitisation of Pain in Osteoarthritis | ||
Medical condition: Osteoarthritis of the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001638-37 | Sponsor Protocol Number: COX2M3M | Start Date*: 2022-03-28 |
Sponsor Name:Semmelweis Egyetem Fogorvostudományi Kar Arc- Állcsont- Szájsebészeti és Fogászati Klinika, Budapest | ||
Full Title: Comparison of the preventive painkiller effect of etoricoxib and celecoxib after M3M surgery: A randomized, double-masked clinical trial | ||
Medical condition: postoperative pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015383-33 | Sponsor Protocol Number: Eto-Dic-01 | Start Date*: 2010-08-30 | |||||||||||
Sponsor Name:Freistaat Bayern, vertreten durch die Universität Regensburg | |||||||||||||
Full Title: Die perioperative Anwendung von Etoricoxib verglichen mit Diclofenac bei Patienten nach Implantation einer Hüftgelenkstotalendoprothese, prospektive, doppelt blinde Phase IIIb Studie | |||||||||||||
Medical condition: In this clinical trial we will investigate patients who suffer from primary or secondary coxarthrosis where an implantation of a total hip joint endoprosthesis is indicated. It will be analyzed whe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003379-28 | Sponsor Protocol Number: 0663-098 | Start Date*: 2009-03-11 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Randomized, Double-Blind, Placebo- and Active-Comparator-Controlled, Multiple-Dose, Clinical Trial to Study the Safety and Efficacy of MK-0663/Etoricoxib and Ibuprofen in the Treatment ... | |||||||||||||
Medical condition: Pain after total knee replacement | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) LT (Completed) EE (Completed) HU (Completed) SI (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022873-32 | Sponsor Protocol Number: MRK008b-2010 | Start Date*: 2010-12-14 |
Sponsor Name:Analgesic Solutions | ||
Full Title: An Enriched Enrollment, Double Blind, Placebo-Controlled, Parallel Group, Randomized Withdrawal Trial to Evaluate the Efficacy, Tolerability and Safety of Etoricoxib (Arcoxia) in Patients with Mode... | ||
Medical condition: Patients with Neuropathic Pain. In the first instance, the investigator will aim to recruit patients with post herpetic neuralgia. If insufficient patients with post herpetic neuralgia are recruite... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013786-25 | Sponsor Protocol Number: IISP 35166 | Start Date*: 2010-04-19 | |||||||||||
Sponsor Name:Northumbria Healthcare NHS Foundation Trust | |||||||||||||
Full Title: Comparison of the effect of Etoricoxib and Diclofenac on early morning activity in RA. | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000451-17 | Sponsor Protocol Number: 1-06 | Start Date*: 2006-05-08 |
Sponsor Name:Marienkrankenhaus Soest | ||
Full Title: Etoricoxib als präemptives Analgetikum bei therapeutischen Arthroskopien | ||
Medical condition: Kniegelenkserkrankenungen, die einer therapeutischen Arthroskopie bedürfen | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021604-16 | Sponsor Protocol Number: etoricoxib-fast-track-2010 | Start Date*: 2010-12-08 | |||||||||||
Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
Full Title: A double-blind, randomized, placebo controlled study to evaluate the effectiveness of etoricoxib as an additive analgesic to epidural analgesia in colon or rectum fast-track surgery | |||||||||||||
Medical condition: Post-operative pain after laparoscopic colon or rectum surgery in fast-track design | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000684-16 | Sponsor Protocol Number: reboundpainplexus | Start Date*: 2016-05-25 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Brachial plexus block and rebound pain after radius fixation with a polar plate. | ||
Medical condition: Pain after radius fracture fixation by a volar plate. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002611-29 | Sponsor Protocol Number: MEL001 | Start Date*: 2012-04-04 |
Sponsor Name:Freistaat Bayern | ||
Full Title: A prospective phase I and consecutive phase II, twoarm, randomized multi-center trial of temsirolimus in combination with pioglitazone, etoricoxib and metronomic low-dose trofosfamide versus dacarb... | ||
Medical condition: metastatic melanoma or metastatic uveal carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017309-12 | Sponsor Protocol Number: GRE-2009-01 | Start Date*: 2010-02-18 | |||||||||||
Sponsor Name:FUNDACIÓN ESPAÑOLA DE REUMATOLOGÍA (FER) | |||||||||||||
Full Title: Evaluación de la respuesta a etoricoxib en pacientes con Espondilitis Anquilosante (EA) e inadecuada respuesta > o = a 2 AINES | |||||||||||||
Medical condition: Espondilitis Anquilosante | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020547-13 | Sponsor Protocol Number: 201001 | Start Date*: 2011-08-24 | |||||||||||
Sponsor Name:Foot and Ankle Surgical center | |||||||||||||
Full Title: A randomized study comparing etoricoxib and diclofenac sodium in post hallux valgus surgery pain | |||||||||||||
Medical condition: Postoperative pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000218-19 | Sponsor Protocol Number: CSTI571BDE59 | Start Date*: 2008-05-21 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A single stage phase II, multi-centre, open label study of Glivec in combination with pioglitazone, etoricoxib, dexamethasone and low-dose treosulfane for anti-inflammatory and angiostatic treatmen... | |||||||||||||
Medical condition: prostrate carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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