- Trials with a EudraCT protocol (582)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
582 result(s) found for: Joint disorders.
Displaying page 1 of 30.
| EudraCT Number: 2008-006141-12 | Sponsor Protocol Number: Start | Start Date*: 2008-11-14 | |||||||||||
| Sponsor Name:UMCG | |||||||||||||
| Full Title: Arthrocentesis as initial treatment of arthropathy of the temporomandibular joint | |||||||||||||
| Medical condition: Arthropathy of the temporomandibular joint | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002123-41 | Sponsor Protocol Number: anakinrapain1 | Start Date*: 2013-10-21 | |||||||||||
| Sponsor Name:Lovisenberg Diaconal Hospital | |||||||||||||
| Full Title: Effects of intraarticular IL1-Ra on pain and inflammatory mediators after knee arthroscopy –a double blind, placebo controlled study using microdialysis technique | |||||||||||||
| Medical condition: Post operative pain after diagnostic or therapeutic knee arthroscopy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003395-23 | Sponsor Protocol Number: HK_VL_08_2014 | Start Date*: 2015-01-20 | |||||||||||
| Sponsor Name:Section for Surgical Pathophysiology, Rigshospitalet | |||||||||||||
| Full Title: Effect of preoperative intravenous highdose methylprednisolone on quadriceps muscle function, endothelial function, complement activation and glucose homeostasis in patients scheduled for total kne... | |||||||||||||
| Medical condition: Knee joint arthrosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002744-40 | Sponsor Protocol Number: HK_EA_02_2014 | Start Date*: 2014-09-23 | |||||||||||
| Sponsor Name:Section For Surgical Pathophysiology, Rigshospitalet | |||||||||||||
| Full Title: Preoperative intraarticular injection of methylprednisolone, in patients scheduled for total knee-arthroplasty | |||||||||||||
| Medical condition: Knee joint arthrosis with hyperalgesia and severe movement related pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000102-19 | Sponsor Protocol Number: HL_VL_01_2015 | Start Date*: 2015-07-07 | |||||||||||
| Sponsor Name:Section for Surgical Pathophysiology, Rigshospitalet | |||||||||||||
| Full Title: Effect of preoperative intravenous highdose methylprednisolone on orthostatic intolerance, sleeping pattern, glucose homeostasis and immune signaling in patients scheduled for total hip-arthroplasty | |||||||||||||
| Medical condition: Hip joint arthrosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-006036-23 | Sponsor Protocol Number: CMM-PRGF/ART | Start Date*: 2013-01-14 | |||||||||||
| Sponsor Name:Instituto Científico y Tecnológico de Navarra | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017624-72 | Sponsor Protocol Number: CMM/ART | Start Date*: 2011-10-10 | |||||||||||
| Sponsor Name:Instituto Científico y Tecnológico de Navarra | |||||||||||||
| Full Title: Tratamiento de la Artrosis mediante la inyección intra-articular de Células Madre Mesenquimales de Médula Ósea | |||||||||||||
| Medical condition: Artrosis de rodilla | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020521-40 | Sponsor Protocol Number: DG-EF 01/09 | Start Date*: 2010-06-21 | ||||||||||||||||||||||||||
| Sponsor Name:EPIFARMA S.R.L. | ||||||||||||||||||||||||||||
| Full Title: Evaluation of therapeutic equivalence of diclofenac gel 1% formulation compared to Voltaren emulGel 1% gel in subjects with traumatic pathology: a double blind, randomized, phase III multicentre st... | ||||||||||||||||||||||||||||
| Medical condition: Painful and traumatic inflammation of the joints, muscles, tendons and ligaments. | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2010-024010-61 | Sponsor Protocol Number: DRO/IV-ART-01 | Start Date*: 2011-11-09 | |||||||||||
| Sponsor Name:BIOIBERICA, S.A. | |||||||||||||
| Full Title: NON-INFERIORITY CLINICAL TRIAL ON THE EFFICACY AND SAFETY OF CHONDROITIN SULFATE AND GLUCOSAMINE HYDROCHLORIDE IN COMBINATION VERSUS CELECOXIB IN PATIENTS WITH KNEE OSTEOARTHRITIS | |||||||||||||
| Medical condition: KNEE OSTEOARTHRITIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001465-20 | Sponsor Protocol Number: FMLD-ARSIDOS-48 | Start Date*: 2022-02-11 | |||||||||||
| Sponsor Name:Laboratorios Farmalíder S.A. | |||||||||||||
| Full Title: A double-blind, multicenter, randomized clinical trial to assess the efficacy and safety of Montelukast in patients with erosive / inflammatory arthrosis of the hands | |||||||||||||
| Medical condition: Erosive / inflammatory arthrosis of the hands | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Temporarily Halted) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003413-18 | Sponsor Protocol Number: IM101 | Start Date*: 2014-05-13 | |||||||||||
| Sponsor Name:King’s College London [...] | |||||||||||||
| Full Title: Arthritis Prevention In the Pre-clinical Phase of RA with Abatacept. | |||||||||||||
| Medical condition: The target population for therapeutic intervention will be subjects who carry serum autoantibodies (antibodies to citrullinated protein antigens – ACPA; rheumatoid factor – RF) and who have joint p... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004254-33 | Sponsor Protocol Number: IFH-2014-002 | Start Date*: 2015-02-26 | |||||||||||
| Sponsor Name:Infirst+ HEALTHCARE Ltd | |||||||||||||
| Full Title: A Three Arm Double blind, Randomised Multicentre Study to Investigate the Non-Inferiority of a Soft Gel Capsule of Ibuprofen Lipid Formulation (total daily dose 1200 mg) versus a Standard Soft Gel ... | |||||||||||||
| Medical condition: Episodic knee arthralgia/flaring knee pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010172-21 | Sponsor Protocol Number: ENJOIH01 | Start Date*: 2009-08-27 | |||||||||||
| Sponsor Name:Elena Santagostino | |||||||||||||
| Full Title: An Investigator-sponsored study on rFVIIa prophylaxis in children with haemophilia A and inhibitors Estudio promovido por el investigador sobre profilaxis con rFVIIa en niños con hemofilia A e inh... | |||||||||||||
| Medical condition: Hemofilia A | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: ES (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) FR (Ongoing) PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003790-41 | Sponsor Protocol Number: JAN12006-01 | Start Date*: 2015-05-11 |
| Sponsor Name:Spherium Biomed | ||
| Full Title: Randomised, double-blinded, placebo and active comparator controlled exploratory clinical trial to assess the efficacy and safety of a triple combination of Ibuprofen, magnesium and ascorbic acid ... | ||
| Medical condition: Temporomandibular joint dysfunction syndrome. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004049-26 | Sponsor Protocol Number: MTX-071-P02 | Start Date*: 2017-11-23 | |||||||||||
| Sponsor Name:Mestex | |||||||||||||
| Full Title: Lopain (MTX-071 / resiniferatoxin) An open label, single dose phase Ib/IIa study to determine the safety and clinical effects of intra-articular injections of low doses of Lopain (MTX-071) in pa... | |||||||||||||
| Medical condition: chronic osteoarthritic knee-joint pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004046-18 | Sponsor Protocol Number: CL3-12911-040 | Start Date*: 2012-02-23 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
| Full Title: Knee joint replacement over 5 years in patients with knee osteoarthritis. A long term follow up study in patients of the CL3-12911-018 study. | |||||||||||||
| Medical condition: Osteoarthritis The medical condition investigated in the CL3-12911-018 study was osteoarthritis. The applied CL3-12911-040 trial, CL3-12911-018 follow-up study, is thus performed in osteoarthrit... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Prematurely Ended) AT (Completed) BE (Completed) PL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) DK (Prematurely Ended) LT (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005065-21 | Sponsor Protocol Number: AUX-CC-862 | Start Date*: 2012-03-26 | |||||||||||
| Sponsor Name:Auxilium UK Limited | |||||||||||||
| Full Title: Retreatment of recurrent contractures in joints effectively treated with AA4500 (collagenase clostridium histolyticum [XIAFLEX®/XIAPEX®]) in an Auxilium-sponsored Phase 3 Study in the United States... | |||||||||||||
| Medical condition: Dupuytren's contracture | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002963-92 | Sponsor Protocol Number: CLRX712A12201 | Start Date*: 2020-02-05 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A randomized, placebo-controlled, subject and investigator blinded study investigating the safety, tolerability and preliminary efficacy of 8-week treatment with intra-articular LRX712 to regenerat... | |||||||||||||
| Medical condition: Cartilage injuries | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003232-31 | Sponsor Protocol Number: TDU11685-ACT12505 | Start Date*: 2011-11-03 | |||||||||||
| Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
| Full Title: A two part protocol to assess, using double blind placebo control, the safety, tolerability, and pharmacokinetics of ascending single doses of a new intra-articular administration formulation of SA... | |||||||||||||
| Medical condition: KNEE OSTEOARTHRITIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003467-60 | Sponsor Protocol Number: M13-741 | Start Date*: 2014-06-11 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Phase 2a Study Evaluating the Safety, Efficacy, and Pharmacodynamic Effects of ABT-981 in Patients with Knee Osteoarthritis | |||||||||||||
| Medical condition: Adult male and female patients with mild to moderate, symptomatic, radiographic and inflammatory osteoarthritis of the knee | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) GB (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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