- Trials with a EudraCT protocol (94)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
94 result(s) found for: Arthralgia.
Displaying page 1 of 5.
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: 2014-000555-93 | Sponsor Protocol Number: ARIAA | Start Date*: 2014-08-20 | |||||||||||
Sponsor Name:University Hospital Erlangen | |||||||||||||
Full Title: Abatacept reversing subclinical Inflammation as measured by MRI in ACPA positive Arthralgia | |||||||||||||
Medical condition: Patients with ACPA (anti citrullinated peptide antibodies) positive arthralgia and OMERACT RAMRIS synovitis (synovialitis or tenosynovitis) or osteitis but without clinical arthritis, defined by jo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004472-35 | Sponsor Protocol Number: TREAT-EARLIER | Start Date*: 2015-03-02 |
Sponsor Name:Leiden University medical Centre | ||
Full Title: TREAT EARLY ARTHRALGIA TO REVERSE OR LIMIT IMPENDING EXACERBATION TO RHEUMATOID ARTHRITIS | ||
Medical condition: Arthralgia of hands or feet of patients that are suspect to progress to reumatoid arthritis according to the treating rheumatologist and because of subclinical inflammation on MRI of hands and feet... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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: 2018-001114-15 | Sponsor Protocol Number: 01-13032018 | Start Date*: 2018-09-18 |
Sponsor Name:VU Medical Center, department of Rheumatology | ||
Full Title: Positron emission tomography with macrophage targeting to select individuals at risk for rheumatoid arthritis. | ||
Medical condition: Rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
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: 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: 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: 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: 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: 2009-010955-29 | Sponsor Protocol Number: 10031983 | Start Date*: 2009-07-13 |
Sponsor Name:Division of Clinically Immunology and Rheumatology, AMC | ||
Full Title: Prevention of clinically manifest rheumatoid arthritis by B cell directed therapy in the earliest phase of the disease. | ||
Medical condition: Pre-clinical RA patients with a high risk on developing the disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-009856-19 | Sponsor Protocol Number: 42160443PAI2004AmINT-2 | Start Date*: 2009-12-17 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Moderate to Severe Knee ... | |||||||||||||
Medical condition: moderate to severe, chronic, knee or hip pain from osteoarthritis (OA) that is not adequately controlled by standard pain therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000283-27 | Sponsor Protocol Number: VX04-765-201 | Start Date*: 2004-07-19 |
Sponsor Name:Vertex Pharmaceuticals Incorporated | ||
Full Title: A Pilot Open-Label Study to Investigate the Safety and Anti-inflammatory Effects of VX-765, an Orally Administered Interleukin-1β Converting Enzyme Inhibitor, in Patients with Muckle-Wells Syndrome | ||
Medical condition: Muckle-Wells syndrome | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004488-33 | Sponsor Protocol Number: Prada2500? | Start Date*: 2020-01-30 | ||||||||||||||||
Sponsor Name:Niels Bang | ||||||||||||||||||
Full Title: Botox injektion in the hip joint for pain relief and diagnosis of pain lokalisation. | ||||||||||||||||||
Medical condition: Patients with hip pain 6 month after operation with periacetabular osteotomi for dysplastic hip. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001235-31 | Sponsor Protocol Number: DEALSZ-2019-001 | Start Date*: 2019-11-26 | |||||||||||
Sponsor Name:Charité – Universitätsmedizin Berlin | |||||||||||||
Full Title: Factor XII-associated cold autoinflammatory syndrome (FACAS) linked to kallikrein-kinin pathology: Proof of concept treatment with Lanadelumab (DX-2930) | |||||||||||||
Medical condition: Lanadelumab in patients with Factor XII-associated cold autoinflammatory syndrome (FACAS) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024156-28 | Sponsor Protocol Number: CACZ885DDE03T | Start Date*: 2011-05-16 | |||||||||||
Sponsor Name:Charité - University Hospital of Berlin | |||||||||||||
Full Title: A multi-center, double-blind, placebo-controlled phase II study of the efficacy and safety of canakinumab in subjects with Schnitzler syndrome | |||||||||||||
Medical condition: Schnitzler syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001555-38 | Sponsor Protocol Number: 104745 | Start Date*: 2005-06-14 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: Open Immunization Study to Determine the Reactogenicity and Immunogenicity of Fluarix/ Influsplit SSW 2005/2006 in Persons as of 18 Years of Age | ||
Medical condition: Immunization against Influenza in healthy male and female subjects aged over 18 years | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-003268-25 | Sponsor Protocol Number: RC31/19/0504 | Start Date*: 2020-11-09 | |||||||||||
Sponsor Name:CHU Toulouse | |||||||||||||
Full Title: Hydroxychloroquine in isolated cutaneous mastocytosis patients or indolent systemic mastocytosis with associated skin involvement patients: proof of concept study | |||||||||||||
Medical condition: mastocytosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001981-24 | Sponsor Protocol Number: MTX-071-P01 | Start Date*: 2016-02-04 | |||||||||||||||||||||
Sponsor Name:Mestex | |||||||||||||||||||||||
Full Title: Lopain (MTX-071 / resiniferatoxin) An open label, dose-escalating phase I/IIa study to determine the safety and clinical effects of intra-articular injections of Lopain (MTX-071) in patients wi... | |||||||||||||||||||||||
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: 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 |
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