- Trials with a EudraCT protocol (190)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
190 result(s) found for: Arthropathy.
Displaying page 1 of 10.
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: 2020-003602-31 | Sponsor Protocol Number: TRM-201-HA-301 | Start Date*: 2021-12-15 |
Sponsor Name:Tremeau Pharmaceuticals, Inc. | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Phase III Study with a Long-Term, Open-label Extension to Evaluate the Efficacy and Safety of TRM-201 (Rofecoxib) in Patients with He... | ||
Medical condition: Hemophilic Arthropathy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) PL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003148-11 | Sponsor Protocol Number: MoA-Ustekinumab | Start Date*: 2015-01-29 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Mechanism of action study of Ustekinumab treatment in psoriatic arthritis: Impact on cellular and molecular pathways of synovial inflammation and tissue remodeling | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: psoriatic arthritis | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||
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: 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: 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: 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: 2018-003724-36 | Sponsor Protocol Number: CODIF-008 | Start Date*: 2020-04-24 | |||||||||||
Sponsor Name:Ole Lander Svendsen | |||||||||||||
Full Title: The DENOCHARCOT trial Efficacy of treatment with DENOsumab of an acute CHARCOT foot in patients with diabetes. A multicenter, double-blind, randomized, placebo-controlled trial. | |||||||||||||
Medical condition: acute Charcot foot (Charcot arthropathy; ICD-10: DM14.6) in patients with diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002176-25 | Sponsor Protocol Number: 1510150 | Start Date*: 2016-04-01 |
Sponsor Name:Royal Devon and Exeter NHS Foundation Trust | ||
Full Title: Do ultrasound guided botulinum A injections relieve pain in rotator cuff arthropathy? | ||
Medical condition: Rotator Cuff Tear Arthropathy | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (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: 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: 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: 2019-001773-90 | Sponsor Protocol Number: MiCROBPsA | Start Date*: 2020-03-10 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SANT'ANDREA | |||||||||||||
Full Title: Metagenomic analysis of the gut microbiota in patients with psoriatic arthritis upon treatment with the jak-stat inhibitor tofacitinib: correlations with immunological, clinical and imaging markers | |||||||||||||
Medical condition: Psoriatic Arthritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000814-31 | Sponsor Protocol Number: CAIN457F3302 | Start Date*: 2016-08-03 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: MAXIMISE (Managing AXIal Manifestations in Psoriatic Arthritis with SEcukinumab), a randomized, double-blind, placebo-controlled, multicenter, 52 week study to assess the efficacy and safety of sec... | |||||||||||||
Medical condition: Axial Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) FR (Completed) GB (Completed) HU (Completed) EE (Completed) IE (Completed) BE (Completed) FI (Completed) DK (Prematurely Ended) DE (Completed) BG (Completed) GR (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002326-49 | Sponsor Protocol Number: I1F-MC-RHAP | Start Date*: 2013-11-05 | |||||||||||
Sponsor Name:Eli Lilly & Company | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Active and Placebo-Controlled 24-Week Study Followed by Long-Term Evaluation of Efficacy and Safety of Ixekizumab (LY2439821) in Biologic Disease-Modifying ... | |||||||||||||
Medical condition: Arthritic Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) BE (Completed) EE (Completed) BG (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002433-22 | Sponsor Protocol Number: I1F-MC-RHBF | Start Date*: 2015-11-12 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3, Multicenter Study with a 36-Week Open-Label Period Followed by a Randomized Double-Blind Withdrawal Period from Week 36 to Week 104 to Evaluate the Long Term Efficacy and Safety of Ixeki... | |||||||||||||
Medical condition: Arthritic Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) EE (Completed) CZ (Completed) GB (Completed) ES (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003849-10 | Sponsor Protocol Number: CAIN457F2336 | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase III, randomized, double-blind, placebo-controlled multicenter study of subcutaneous secukinumab (150 mg) in pre-filled syringe, with or without loading regimen, to demonstrate efficacy, saf... | |||||||||||||
Medical condition: Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) BE (Completed) BG (Completed) DE (Completed) GB (Completed) PL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000465-32 | Sponsor Protocol Number: CNTO1959PSA4002 | Start Date*: 2021-08-11 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 4, Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Bio-naive Participants with Active Psoriat... | |||||||||||||
Medical condition: Active Psoriatic Arthritis Axial Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) DE (Trial now transitioned) HU (Trial now transitioned) PT (Trial now transitioned) IT (Trial now transitioned) BG (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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