- Trials with a EudraCT protocol (744)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
744 result(s) found for: Joint Pain.
Displaying page 1 of 38.
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: 2009-015378-36 | Sponsor Protocol Number: ART1 | Start Date*: 2009-12-23 | |||||||||||||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||||||||||||
Full Title: Effect of anastrozole on arthralgia and the effect of glucosamine sulphate supplementation in postmenopausal women with arthralgia in the IBIS-II breast cancer prevention trial | |||||||||||||||||||||||
Medical condition: Relief of arthralgia, joint symptoms/stiffness with glucosamine sulphate | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
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: 2014-002744-40 | 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: 2005-004279-39 | Sponsor Protocol Number: BUP4004 | Start Date*: 2006-01-25 | |||||||||||
Sponsor Name:Napp Pharmaceuticals Limited | |||||||||||||
Full Title: An open, randomised, multicentre study to compare buprenorphine transdermal delivery system (BTDS) with standard treatment in elderly subjects with OA of the hip and/or knee. | |||||||||||||
Medical condition: Severe osteoarthritic pain of the hip(s) and/or knee(s) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003513-40 | Sponsor Protocol Number: Bupi-Cata-TYKS-version 1.0. | Start Date*: 2006-08-21 | |||||||||||
Sponsor Name:Kalevi Pihlajamäki | |||||||||||||
Full Title: Intrathecal bupivacaine and clonidine for ambulatory knee arthroscopy | |||||||||||||
Medical condition: Patients are submitted for ambulatory knee arthroscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004921-33 | Sponsor Protocol Number: R475-OA-1758 | Start Date*: 2018-11-09 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Effects of Fasinumab on Peripheral Nerve Function in Patients with Pain Due to Osteoarthritis of the Hip or Knee | ||||||||||||||||||
Medical condition: Pain due to osteoarthritis of the hip or knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003365-34 | Sponsor Protocol Number: Artralgia1 | Start Date*: 2013-10-25 |
Sponsor Name:Specialisttandvårdskliniken Västmanlands sjukhus Västerås | ||
Full Title: Pain relief following an intra-articular single dose metylprednisolon vs. placebo on temporomandibular joint artralgia patientens. A randomized controlled blinded multicenter study. | ||
Medical condition: Artralgia of the jaw joint | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
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: 2006-006911-60 | Sponsor Protocol Number: 42801PAI3001 | Start Date*: 2007-06-15 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: Randomised, double-blind, placebo-controlled, parallel-group trial to investigate the analgesic effect of OROS hydromorphone hydrochloride in comparison with placebo in subjects with moderate to se... | |||||||||||||
Medical condition: moderate to severe pain induced by osteoarthritis of the hip or the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
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: 2019-002717-19 | Sponsor Protocol Number: OLT1177-08 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:Olatec Therapeutics LLC | |||||||||||||
Full Title: A Multi-Center Phase 2/3 Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Safety and Efficacy Study of Dapansutrile Tablets in Subjects with an Acute Gout Flare | |||||||||||||
Medical condition: Treatment of Acute Gout Flare | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) 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: 2005-003287-28 | Sponsor Protocol Number: lustgas 2 | Start Date*: Information not available in EudraCT |
Sponsor Name:Queen Silvia's Childrens hospital | ||
Full Title: Nitrous oxide for analgesia and sedation during procedural pain in children -Efficacy ina short and long perspective regarding joint injections | ||
Medical condition: Juvenile Idiopathic Arthrithis (JIA) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
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: 2006-004514-40 | Sponsor Protocol Number: KF5503/33-R331333-PAI-3002 | Start Date*: 2007-02-14 | |||||||||||
Sponsor Name:Johnson & Johnson Pharamceutical Research & Development, L.L.C. | |||||||||||||
Full Title: A Randomized, Double-Blind, Active- And Placebo-Controlled, Parallel Group, Multicenter Study To Evaluate The Efficacy And Safety of Multiple Doses of CG5503 Immediate Release Formulation In Subjec... | |||||||||||||
Medical condition: Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 2018-000818-37 | Sponsor Protocol Number: MTX-071-P03 | Start Date*: 2018-06-28 | |||||||||||||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, single dose phase IIb exploratory study to document the clinical effects and safety of intra-articular injections of Lopain (MTX-071) in patients wit... | |||||||||||||||||||||||
Medical condition: chronic osteoarthritic knee joint pain | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) SK (Completed) HR (Completed) | |||||||||||||||||||||||
Trial results: View results |
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: 2012-002518-38 | Sponsor Protocol Number: KETASONE | Start Date*: 2013-07-04 | |||||||||||
Sponsor Name:Hospital Universitari de Girona Dr. Josep Trueta | |||||||||||||
Full Title: KETAMINE AND DEXAMETHASONE IN THE MANAGEMENT OF LOW BACK PAIN DURING ARTHRODESIS | |||||||||||||
Medical condition: Pain in the lumbar arthrodesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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