- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
18 result(s) found for: Dexketoprofen.
Displaying page 1 of 1.
EudraCT Number: 2012-004548-31 | Sponsor Protocol Number: DEX-TRA-05 | Start Date*: 2013-04-15 | |||||||||||
Sponsor Name:Menarini Ricerche S.p.A. | |||||||||||||
Full Title: A randomized, double-blind, placebo and active-controlled, parallel-group study to evaluate the analgesic efficacy and safety of dexketoprofen trometamol and tramadol hydrochloride oral fixed combi... | |||||||||||||
Medical condition: Treatment of moderate to severe acute pain after elective unilateral total hip arthoplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Completed) HU (Completed) LV (Completed) LT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004545-32 | Sponsor Protocol Number: DEX-TRA-04 | Start Date*: 2013-02-27 | |||||||||||
Sponsor Name:Menarini Ricerche S.p.A. | |||||||||||||
Full Title: A randomized, double-blind, placebo and active-controlled, parallel-group study to evaluate the analgesic efficacy and safety of dexketoprofen trometamol and tramadol hydrochloride oral fixed combi... | |||||||||||||
Medical condition: Treatment of moderate to severe acute pain following abdominal hysterectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SK (Completed) HU (Completed) ES (Completed) LV (Completed) PL (Completed) LT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000414-35 | Sponsor Protocol Number: AITT2016/2 | Start Date*: 2017-04-21 | |||||||||||
Sponsor Name:University of Debrecen Faculty of Medicine, Department of | |||||||||||||
Full Title: Administration of Preemptive Analgesia by Dexketoprofen to prevent Acute and Chronic Postcraniotomy Headache. A randomized Placebo Controlled, Single-center Study | |||||||||||||
Medical condition: Headache | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002085-39 | Sponsor Protocol Number: 2013-03-23 | Start Date*: 2013-07-09 | |||||||||||
Sponsor Name:Kuopio University Hospital | |||||||||||||
Full Title: Effect of dexketoprofen on analgesic concentration of oxycodone after laparoscopic cholecystectomy | |||||||||||||
Medical condition: Cholelithiasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022798-32 | Sponsor Protocol Number: DEX-TRA 02 | Start Date*: 2010-12-14 | |||||||||||
Sponsor Name:Menarini Ricerche S.p.A. | |||||||||||||
Full Title: DOUBLE-BLIND, RANDOMISED, PLACEBO AND ACTIVE CONTROLLED, PARALLEL GROUP STUDY TO EVALUATE THE ANALGESIC EFFECT OF A SINGLE ORAL ADMINISTRATION OF FOUR DIFFERENT COMBINATION DOSES OF DKP.TRIS WITH T... | |||||||||||||
Medical condition: Severe pain following impacted third mandibular molar tooth extraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) HU (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004152-22 | Sponsor Protocol Number: DEX-TRA-06 | Start Date*: 2016-03-01 | |||||||||||
Sponsor Name:MENARINI RICERCHE S.p.A. | |||||||||||||
Full Title: Analgesic efficacy of oral dexketoprofen trometamol/tramadol hydrochloride versus tramadol hydrochloride/paracetamol: a randomised, double-blind, placebo and active-controlled, parallel group study... | |||||||||||||
Medical condition: moderate to severe acute pain after removal of impacted lower third molar | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002982-20 | Sponsor Protocol Number: 2013-01-07 | Start Date*: 2013-08-28 | ||||||||||||||||
Sponsor Name:Merja Kokki | ||||||||||||||||||
Full Title: | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000866-38 | Sponsor Protocol Number: MeFi/05/Dex-Mig/01 | Start Date*: 2005-08-05 | |||||||||||
Sponsor Name:A. MENARINI I.F.R. | |||||||||||||
Full Title: DEXKETOPROFEN TROMETAMOL IN ATTACK THERAPY OF MIGRAINE. | |||||||||||||
Medical condition: ATTACK THERAPY OF MIGRAINE. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001789-42 | Sponsor Protocol Number: IC01/04/DKP | Start Date*: 2004-12-07 | |||||||||||
Sponsor Name:Laboratorios Menarini, S.A. | |||||||||||||
Full Title: A MULTICENTRE CLINICAL TRIAL EVALUATING THE ANALGESIC EFFICACY AND SAFETY OF DEXKETOPROFEN TROMETAMOL (50 mg i.v. FOLLOWED BY AN ORAL DOSAGE OF 25 mg t.i.d.) VERSUS METAMIZOL (2 g i.v. and 575 mg t... | |||||||||||||
Medical condition: Patients who underwent ambulatory surgery consisting in unilateral inguinal mesh hernioplasty | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001373-26 | Sponsor Protocol Number: IC01/03/DKP(12-Kef) | Start Date*: 2004-11-15 | |||||||||||
Sponsor Name:Laboratorios Menarini, S.A | |||||||||||||
Full Title: Multicentre clinical trial to evaluate the efficacy and safety of dexketoprofen trometamol (50 mg t.i.d.) versus ketorolac (30 mg t.i.d.) and placebo by intravenous route, as part of balanced analg... | |||||||||||||
Medical condition: elective orthopedic surgery (hip arthroplasty) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006182-32 | Sponsor Protocol Number: ANESBURN_1017 | Start Date*: 2009-06-03 |
Sponsor Name:Anaesthesiology Department. Universitary Hospital Vall d'Hebron, Barcelona. | ||
Full Title: Ensayo clínico controlado y aleatorizado para evaluar el efecto de los gabapentinoides sobre el dolor agudo postoperatorio en pacientes quemados | ||
Medical condition: Postoperative pain in burned patients with a burn excision area between 2 and 12 % of total body surface area. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011577-32 | Sponsor Protocol Number: LUMI/09/Fro+Dex-Mig/001 | Start Date*: 2009-05-29 | ||||||||||||||||
Sponsor Name:LUSOFARMACO | ||||||||||||||||||
Full Title: Comparison between frovatriptan plus different treatment regimens of dexketoprofen (25 mg and 37.5 mg) and frovatriptan alone in the acute treatment of migraine without aura and migraine with aura ... | ||||||||||||||||||
Medical condition: migraine with or without aura | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003656-37 | Sponsor Protocol Number: MEIN/18/DEX-LBP/001 | Start Date*: 2020-06-04 | |||||||||||
Sponsor Name:Menarini International Operations Luxembourg SA | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, parallel arm group study to evaluate the analgesic efficacy and safety of dexketoprofen trometamol and tramadol hydrochloride oral fixed dose combina... | |||||||||||||
Medical condition: Low back pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) PL (Completed) ES (Completed) HU (Completed) LV (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003051-37 | Sponsor Protocol Number: 2013-07-03 | Start Date*: 2013-08-28 | ||||||||||||||||
Sponsor Name:Kuopion yliopistollinen sairaala | ||||||||||||||||||
Full Title: | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003346-16 | Sponsor Protocol Number: 2012-01-ANE | Start Date*: 2017-02-16 |
Sponsor Name:Hospital Universitari Sagrat cor | ||
Full Title: Comparative study between continuous perfusion and split doses in the treatment of postoperative pain | ||
Medical condition: Analgesic efficacy in postoperative acute pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001930-26 | Sponsor Protocol Number: LEOC/FJD-14/01 | Start Date*: 2014-10-10 | |||||||||||
Sponsor Name:INSTITUTO DE INVESTIGACION SANITARIA FUNDACION JIMENEZ DIAZ | |||||||||||||
Full Title: A randomized, evaluator blinded clinical trial to compare clinical efficacy of four different analgesic strategies in patients undergoing Extracorporeal Shock Wave Lithotripsy (ESWL). | |||||||||||||
Medical condition: Pain in Nephrolithiasis in whom Extracorporeal shock wave lithotripsy is indicated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001146-29 | Sponsor Protocol Number: 1 | Start Date*: 2016-01-12 |
Sponsor Name:Hospital Central de la Defensa | ||
Full Title: Selective local anesthesia versus a combined medication injection with corticosteroids in degenerartive spine | ||
Medical condition: Degenerative spine pain when there are no indications for surgical treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000566-36 | Sponsor Protocol Number: 14072010 | Start Date*: 2011-09-20 | |||||||||||
Sponsor Name:Hannu Kokki | |||||||||||||
Full Title: Laskimoon annetun ketoprofeenin ja deksketoprofeenin aiheuttama kirvely | |||||||||||||
Medical condition: Potilaat, joille on tarkoitus tehdä ei-päivystyksellinen toimenpide, ja joilla on tarkoitus käyttää laskimoon annettavaa ketoprofeenia ennakoivana kipulääkityksenä. Potilaiden tulee kuulua anestesi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
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