- Trials with a EudraCT protocol (117)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
117 result(s) found for: Synovitis.
Displaying page 1 of 6.
EudraCT Number: 2017-003425-15 | Sponsor Protocol Number: 2017 | Start Date*: 2017-11-10 | |||||||||||
Sponsor Name:Videncenter for Reumatologi og Rygsygdomme, Rigshospitalet | |||||||||||||
Full Title: Patients with rheumatoid arthritis and synovitis treated with ultrasound guided intraarticular or intramuscular glucocorticoid injection - A randomised, double-blind, controlled study (Panguian) | |||||||||||||
Medical condition: Treatment of synovitis among rheumatoid arthritis patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004006-26 | Sponsor Protocol Number: H-4-2013-095 | Start Date*: 2013-12-18 | |||||||||||
Sponsor Name:Knowledge Centre for Rheumatology and Back Diseases | |||||||||||||
Full Title: Optical images for monitoring treatment changes in rheumatoid arthritis – a longitudinal study with Rheumascan | |||||||||||||
Medical condition: Detection of synovitis and tenosynovitis in the hands of patients with rheumatoid arthritis; Diagnostic performance of optical imaging in comparison with ultrasound and magnetic resonance imaging. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003486-34 | Sponsor Protocol Number: 39132 | Start Date*: 2013-11-04 | |||||||||||
Sponsor Name:Knowledge Centre for Rheumatology and Back Diseases | |||||||||||||
Full Title: Systemic versus ultrasound-guided local glucocorticoid treatment, among rheumatoid arthritis patients with tenosynovitis - a randomized double blind study | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000547-17 | Sponsor Protocol Number: FPA008-002 | Start Date*: 2015-11-18 | |||||||||||
Sponsor Name:Five Prime Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 1/2 Study of FPA008, an anti-CSF1 Receptor Antibody, in Patients with Pigmented Villonodular Synovitis (PVNS)/ Diffuse Type Tenosynovial Giant Cell Tumor (dt-TGCT) | |||||||||||||
Medical condition: Pigmented villonodular synovitis (PVNS)/Diffuse Type Tenosynovial Giant Cell Tumor (dt-TGCT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000993-20 | Sponsor Protocol Number: TW77 | Start Date*: 2014-12-04 |
Sponsor Name:Center for Research and Development Uppsala University/County Council of Gävleborg | ||
Full Title: Dosing of intraarticular triamcinolone hexacetonid for knee synovitis in chronic polyarthritis | ||
Medical condition: Psoriatic arthritis and rheumatoid arthritis with synovitis of the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018869-29 | Sponsor Protocol Number: ET2009-095 | Start Date*: 2010-07-29 | |||||||||||
Sponsor Name:CENTRE LEON BERARD | |||||||||||||
Full Title: Phase II study of nilotinib efficacy in Pigmented Villo-Nodular Synovitis / Tenosynovial Giant Cell Tumor (PVNS / TGCT) | |||||||||||||
Medical condition: Patients with inoperable Pigmented Villonodular Synovitis / Tenosynovial Giant Cell Tumour (PVNS/TGCT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Completed) NL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000101-28 | Sponsor Protocol Number: AMB-051-07 | Start Date*: 2022-12-08 | |||||||||||
Sponsor Name:AmMax Bio, Inc. | |||||||||||||
Full Title: A Phase 2, Open-Label, Adaptive, Dose-Ranging Study with Long-Term Extension to Evaluate the Safety, Tolerability, Efficacy, and Pharmacokinetics of Intra-articular AMB-05X Injections in Subjects w... | |||||||||||||
Medical condition: Tenosynovial Giant Cell Tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) IT (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012218-30 | Sponsor Protocol Number: ML22648 | Start Date*: 2009-10-06 |
Sponsor Name:Roche Farmacêutica Química, Lda. | ||
Full Title: A randomized, double-blind, placebo-controlled study to assess the efficacy of tocilizumab (TCZ) + non-biological DMARD in reducing synovitis as measured by magnetic resonance imaging (MRI) at 12 w... | ||
Medical condition: Men and women > 18 years of age with RA who are currently experiencing an inadequate clinical response to a stable dose of non-biologic DMARDs (at least 12 weeks) and with MRI documented synovitis ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (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: 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: 2004-002620-18 | Sponsor Protocol Number: IM101-046 | Start Date*: 2005-05-13 |
Sponsor Name:Bristol-Myers Squibb International Corporation | ||
Full Title: A Multi-National Randomized, Double-Blind, Exploratory Study of Abatacept versus Placebo in Preventing the Development of Rheumatoid Arthritis in Adult Subjects with Undifferentiated Inflammatory A... | ||
Medical condition: Rheumatoid Arthritis, NOS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) BE (Completed) IT (Completed) ES (Completed) | ||
Trial results: Removed from public view |
EudraCT Number: 2018-004558-30 | Sponsor Protocol Number: BIOP-US | Start Date*: 2019-05-16 | |||||||||||
Sponsor Name:Fundación Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz | |||||||||||||
Full Title: Synovial ultrasound as primary outcome in a 3-arm, randomized, open-label, parallel active controlled, multicenter international study comparing baricitinib, alone and combined with MTX versus TNF-... | |||||||||||||
Medical condition: rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PT (Completed) DK (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002394-38 | Sponsor Protocol Number: CAIN457F2354 | Start Date*: 2016-05-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 52-week, multicenter study to assess the time course of response to secukinumab on joint inflammation using Power Doppler ultrasonography in patients with active psoriatic arthritis | |||||||||||||
Medical condition: Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IE (Completed) ES (Completed) HU (Completed) BE (Completed) NO (Completed) FR (Completed) AT (Completed) NL (Completed) CZ (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020890-18 | Sponsor Protocol Number: A3921068 | Start Date*: 2011-02-25 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: AN EXPLORATORY PHASE 2, RANDOMIZED, DOUBLE-BLIND, MULTICENTER STUDY TO ASSESS THE EFFECTS OF TOFACITINIB (CP-690,550) ON MAGNETIC RESONANCE IMAGING ENDPOINTS, IN METHOTREXATE NAÏVE SUBJECTS WITH EA... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001585-33 | Sponsor Protocol Number: MA21056 | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||
Full Title: A randomized, placebo controlled, multicenter clinical study investigating efficacy of rituximab (MabThera®/Rituxan®) in the inhibition of joint structural damage assessed by magnetic resonance ima... | |||||||||||||
Medical condition: Rheumatoid arthritis (RA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) DK (Completed) EE (Completed) FR (Completed) LV (Completed) GR (Completed) NL (Completed) CZ (Completed) ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001625-10 | Sponsor Protocol Number: 0881X1-4437 | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals France | |||||||||||||
Full Title: An Open-Label, Randomized Study To Evaluate The Radiographic Efficacy And Safety Of Enbrel™ (Etanercept) Added To Methotrexate In Comparison With Usual Treatment In Subjects With Moderate Rheumatoi... | |||||||||||||
Medical condition: RHEUMATOID ARTHRITIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Completed) GB (Prematurely Ended) DE (Prematurely Ended) FR (Completed) CZ (Prematurely Ended) AT (Prematurely Ended) PL (Prematurely Ended) DK (Completed) IE (Prematurely Ended) GR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001754-11 | Sponsor Protocol Number: ML 21081 | Start Date*: 2007-08-03 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Pilot study to evaluate the effect of Rituximab in combination with MTX in the inhibition of progression of synovitis, bone marrow edema, and erosions evaluated by magnetic resonance imaging (MRI) ... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004878-41 | Sponsor Protocol Number: RR08-8686 | Start Date*: 2009-10-23 |
Sponsor Name:University of Leeds | ||
Full Title: ASUS: Abatacept in Seronegative Undifferentiated arthritis Study Prospective, Single-centre, Pilot Study Assessing the Efficacy of Abatacept in Anti-CCP Negative Undifferentiated Inflammatory Arthr... | ||
Medical condition: Undifferentiated Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004354-15 | Sponsor Protocol Number: DANPAPP | Start Date*: 2017-12-13 | ||||||||||||||||
Sponsor Name: Rigshospitalet | ||||||||||||||||||
Full Title: Prevalence, pattern and disease course of arthritis and enthesitis in patients with psoriasis, and the effect of apremilast in subclinical US-defined psoriatic arthritis - A population-based study ... | ||||||||||||||||||
Medical condition: Psoriasis and psoriatic arthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001492-20 | Sponsor Protocol Number: NN8226-4064 | Start Date*: 2014-02-12 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A randomised, active comparator, double-blind, multi centre, parallel, phase 2a trial, investigating the mechanism of action of NNC0109-0012 (anti-IL-20 mAb) through synovial biopsies in subjects w... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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