- Trials with a EudraCT protocol (422)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (32)
422 result(s) found for: Necrosis.
Displaying page 2 of 22.
EudraCT Number: 2010-020061-24 | Sponsor Protocol Number: CACZ885D2203 | Start Date*: 2010-08-24 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label, multicenter, efficacy and safety study of 4-month canakinumab treatment with 5-month follow-up and long-term treatment period in patients with active recurrent or chronic TNF-recepto... | |||||||||||||
Medical condition: TNF-receptor associated periodic syndrome (TRAPS) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004291-35 | Sponsor Protocol Number: CACZ885N2301 | Start Date*: 2014-05-16 | |||||||||||||||||||||
Sponsor Name:Novartis Farma SpA | |||||||||||||||||||||||
Full Title: A randomized, double-blind, placebo controlled study of canakinumab in patients with Hereditary Periodic Fevers (TRAPS, HIDS, or crFMF), with subsequent randomized withdrawal/ dosing frequency redu... | |||||||||||||||||||||||
Medical condition: Hereditary Periodic Fevers (TRAPS, HIDS, or crFMF) | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) ES (Completed) IE (Completed) DE (Completed) BE (Completed) HU (Completed) NL (Completed) GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000788-26 | Sponsor Protocol Number: WATERFALL | Start Date*: 2019-06-10 | |||||||||||
Sponsor Name:Enrique de Madaria | |||||||||||||
Full Title: Effect of early weight-based aggressive versus non-aggressive goal-directed fluid resuscitation in the early phase of acute pancreatitis: an open-label multicenter randomized-controlled trial | |||||||||||||
Medical condition: Acute pancreatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005212-40 | Sponsor Protocol Number: MR080508 | Start Date*: 2008-10-14 | ||||||||||||||||||||||||||
Sponsor Name:Karolinska Institute | ||||||||||||||||||||||||||||
Full Title: Pain mechanisms and fatigue in rheumatoid arthritis (RA) and healthy volunteers. Can antirheumatic and biological therapy affect pain processing and fatigue in RA? | ||||||||||||||||||||||||||||
Medical condition: Rheumatoid arthritis (RA) The overall aim with this project is to investigate central pain mechanisms in RA and healthy controls, and in RA how these are influenced by autonomic neural regulation ... | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001125-15 | Sponsor Protocol Number: ATB-202 | Start Date*: 2018-07-16 | |||||||||||||||||||||
Sponsor Name:Atox Bio | |||||||||||||||||||||||
Full Title: Phase III, randomized, double-blind, placebo controlled, parallel-group, study of AB103 as compared to placebo in patients with necrotizing soft tissue infections (NSTI) | |||||||||||||||||||||||
Medical condition: Necrosis of soft tissue infections (NSTI) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003665-12 | Sponsor Protocol Number: 108/139 | Start Date*: 2009-02-25 | |||||||||||
Sponsor Name:Centro Comunitario de Sangre y Tejidos de Asturias | |||||||||||||
Full Title: ENSAYO CLÍNICO MULTICÉNTRICO, ALEATORIZADO, ABIERTO PARA VALORAR LA EFICACIA Y SEGURIDAD DEL TRATAMIENTO DE HERIDAS QUIRUGICAS DEL PIE DIABÉTICO CON INJERTOS CUTÁNEOS CULTIVADOS | |||||||||||||
Medical condition: Heridas quirúrgicas de pie diabético que evolucionan desfavorablemente | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004756-38 | Sponsor Protocol Number: 2018-1201 | Start Date*: 2019-02-12 |
Sponsor Name:Institut de Cancérologie Lucien Neuwirth | ||
Full Title: Study of thromboelastography during tranexamic acid treatment in preventing bleeding in patients with haematological malignancies presenting severe thrombocytopenia (TTRAP-bleeding) | ||
Medical condition: Malignant hemopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000474-26 | Sponsor Protocol Number: 80570 | Start Date*: 2022-05-09 |
Sponsor Name:Radboudumc | ||
Full Title: Pancreatitis and early omega-3-fatty acid infusion for reduction of organ failure and mortality: a multicenter randomized controlled trial (PLANCTON) | ||
Medical condition: Predicted severe acute pancreatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000454-58 | Sponsor Protocol Number: S53657 | Start Date*: 2012-04-18 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Prospective, monocentre phase I study of sequential infusion of Y90-labeled microspheres and Mitomycine C in patients with chemorefractory liver metastases from breast carcinoma | ||
Medical condition: chemorefractory liver metastases from breast carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004300-65 | Sponsor Protocol Number: AGO/2016/012 | Start Date*: 2017-09-26 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Optimizing the Biologic Treatment Strategy in Rheumatoid Arthritis (RA) Patients that have failed a Tumor Necrosis Factor-alpha (TNFα) blocking Agent by immunoscintigraphy with Technetium-labeled C... | ||
Medical condition: rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000795-14 | Sponsor Protocol Number: 0089 | Start Date*: 2004-07-26 |
Sponsor Name:AstraZeneca | ||
Full Title: A Multicentre, Randomised, Double-blind, Placebo-controlled, Study on the Use of Prophylactic Meropenem Therapy in Subjects with Severe Acute Necrotizing Pancreatitis | ||
Medical condition: severe acute necrotisng pancreatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) LT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003958-85 | Sponsor Protocol Number: IMM-101-007 | Start Date*: 2012-02-03 | |||||||||||
Sponsor Name:Immodulon Therapeutics Ltd | |||||||||||||
Full Title: A Phase II, Single Arm, Investigative Study of IMM-101 in Combination with Radiation Induced Tumour Necrosis in Patients with Previously Treated Colorectal Cancer | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004097-28 | Sponsor Protocol Number: BRD/06/078 | Start Date*: 2007-01-12 | |||||||||||
Sponsor Name:University College Hospitals NHS Foundation Trust/ University College London | |||||||||||||
Full Title: A Phase 1 Trial of Verteporfin Photodynamic Therapy in Unresectable Pancreatic Carcinoma (VERTPAC-01 study) | |||||||||||||
Medical condition: Unresectable pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001257-31 | Sponsor Protocol Number: TACTIDA | Start Date*: 2021-08-25 | |||||||||||
Sponsor Name:Department of Pharmaceutical Biosciences, Uppsala University | |||||||||||||
Full Title: An open, single center two-step trial (A+B), comparing the safety and tolerability of idarubicin 10 mg and 15 mg after separate single hepatic intra-arterial injections of a drug formulation based ... | |||||||||||||
Medical condition: intermediate stage hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003558-26 | Sponsor Protocol Number: ABX464-103 | Start Date*: 2019-12-10 | |||||||||||
Sponsor Name:ABIVAX | |||||||||||||
Full Title: A randomized, double blind, placebo controlled, parallel group, multiple dose, induction study to evaluate the safety, tolerability and optimal dose of ABX464 compared with placebo in patients with... | |||||||||||||
Medical condition: Moderate to Severe Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SI (Completed) CZ (Completed) DE (Completed) SK (Completed) HU (Completed) PL (Completed) BE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019714-24 | Sponsor Protocol Number: 10.002 | Start Date*: 2010-09-02 | ||||||||||||||||
Sponsor Name:Research & Development Department | ||||||||||||||||||
Full Title: A phase II, open label, single site light dose escalation trial of single dose Verteporfin Photodynamic Therapy (PDT) in primary soft tissue sarcoma | ||||||||||||||||||
Medical condition: Primary soft tissue sarcoma in the upper and lower limbs of adults. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002485-11 | Sponsor Protocol Number: EGF104334 | Start Date*: 2006-02-03 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd. | ||
Full Title: A Randomized, Single Blind, Placebo-controlled, Multi-centre, Phase II Study of Lapatinib in Patients with Locally Advanced Squamous Cell Carcinoma of the Head and Neck | ||
Medical condition: Sqamous Cell Carcinoma of the Head & Neck (SCCHN) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003874-30 | Sponsor Protocol Number: ATILA-ictus-2021 | Start Date*: 2022-02-21 | |||||||||||||||||||||||||||||||
Sponsor Name:Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla (FISEVI). | |||||||||||||||||||||||||||||||||
Full Title: RANDOMIZED MULTI-CENTER CLINICAL TRIAL TO ASSESS THE EFFECTIVENESS AND SAFETY OF TIROFIBAN VERSUS INTRAVENOUS ASPIRIN IN PATIENTS WITH ACUTE ISCHEMIC STROKE SECONDARY TO TANDEM INJURY, SUBJECT TO R... | |||||||||||||||||||||||||||||||||
Medical condition: Acute Ischemic Stroke | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005019-42 | Sponsor Protocol Number: ET16-132 | Start Date*: 2018-02-14 | |||||||||||
Sponsor Name:Centre Léon Bérard | |||||||||||||
Full Title: A European, multicenter, randomized, open-label, Phase II trial aiming to assess the clinical and biological activity of an anti-PD-L1 (atezolizumab) in operable localized soft tissue sarcomas pati... | |||||||||||||
Medical condition: localised and operable soft tissue sarcomas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002708-25 | Sponsor Protocol Number: RIVAROXACS3001 (BAY59-7939/13194) | Start Date*: 2008-11-27 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Event-Driven Multicenter Study to Evaluate the Efficacy and Safety of Rivaroxaban in Subjects with a Recent Acute Coronary Syndrome The ATLAS ACS 2 ... | |||||||||||||
Medical condition: Acute Coronary Syndrome (ACS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) LT (Completed) DE (Completed) PT (Completed) SK (Completed) HU (Completed) FR (Completed) DK (Completed) GB (Completed) NL (Completed) ES (Completed) IT (Completed) LV (Completed) CZ (Completed) BG (Completed) BE (Prematurely Ended) GR (Completed) | |||||||||||||
Trial results: View results |
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