- Trials with a EudraCT protocol (422)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
422 result(s) found for: Necrosis.
Displaying page 3 of 22.
| EudraCT Number: 2010-019126-13 | Sponsor Protocol Number: CE-US | Start Date*: 2011-03-04 | |||||||||||
| Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
| Full Title: A PILOT, EXPLORATIVE STUDY TO IDENTIFY CONTRAST-ENHANCED ULTRASOUND (CE-US) PATTERNS THAT CHARACTERIZE ACUTE ALLOGRAFT REJECTION AND OTHER CAUSES OF ACUTE ALLOGRAFT DYSFUNCTION IN RENAL TRANSPLANT ... | |||||||||||||
| Medical condition: Renal transplant | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004988-68 | Sponsor Protocol Number: RINFIS-11 | Start Date*: 2012-08-27 | |||||||||||
| Sponsor Name:Hospital General Universitario de Alicante | |||||||||||||
| Full Title: Saline solution versus Ringer lactate solution in the initial flluid therapy in the acute pancreatitis | |||||||||||||
| Medical condition: FLUID THERAPY IN ACUTE PANCREATITIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001820-51 | Sponsor Protocol Number: BMC2012-PhaseII | Start Date*: 2016-06-27 |
| Sponsor Name:Dekan der medizinischen Fakultät, Universitätsklinikum Frankfurt, Goethe-Universität | ||
| Full Title: BMC2012, Cell based therapy by implanted bone marrow-derived mononuclear cells (BMC) for bone augmentation of plate-stabilized proximal humeral fractures - a randomized, open, multicentric study - ... | ||
| Medical condition: Investigation of cell based therapy by implanted bone marrow-derived mononuclear cells for bone augmentation on osteosynthesis of proximal humeral fractures | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001172-15 | Sponsor Protocol Number: APN01-01-COVID19 | Start Date*: 2020-04-08 |
| Sponsor Name:APEIRON Biologics AG | ||
| Full Title: Recombinant human angiotensin-converting enzyme 2 (rhACE2) as a treat-ment for patients with COVID-19 | ||
| Medical condition: Severe COVID-19 POSITIVE hospitalized male or female, between 18 and ≤ 80 years of age | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) DK (Completed) AT (Completed) GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-006817-12 | Sponsor Protocol Number: 2031-38 | Start Date*: 2022-06-24 |
| Sponsor Name:ASSITANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
| Full Title: Evaluation of the efficacy of an intra-articular injection of autologous microfat combined with autologous platelet-enriched plasma in the treatment of radiocarpal osteoarthritis: a randomized cont... | ||
| Medical condition: radiocarpal osteoarthritis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000080-85 | Sponsor Protocol Number: 17-245 | Start Date*: 2018-11-29 | |||||||||||
| Sponsor Name:CHU CAEN | |||||||||||||
| Full Title: Pilot study of the pharmacokinetic profile of paracetamol subcutaneously versus intravenously in patients receiving palliative care | |||||||||||||
| Medical condition: Major patients in palliative care | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001972-55 | Sponsor Protocol Number: 20963.091.08 | Start Date*: 2009-09-30 |
| Sponsor Name:UMC St Radboud | ||
| Full Title: Efficacy of hyperbaric oxygen therapy in the treatment of late radiation damage, osteoradionecrosis, of the lower jaw. | ||
| Medical condition: Osteoradionecrosis of the jaw due to previous radiotherapy treatment in the head and neck region | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-000679-28 | Sponsor Protocol Number: FAZA-gliomi | Start Date*: 2015-07-13 | |||||||||||
| Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
| Full Title: Prognostic value of 18F-FAZA PET/CT in high grade glioma: comparison with MRI and correlation with hypoxia biomarkers. | |||||||||||||
| Medical condition: Patients with high-grade glioma (III-IV). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002158-59 | Sponsor Protocol Number: SÖSPN | Start Date*: 2018-09-05 |
| Sponsor Name:Södersjukhuset | ||
| Full Title: A prospective study of the safety of peripherally administered norepinephrine during surgery | ||
| Medical condition: Hypotension during general anaesthesia or central blockades | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004817-16 | Sponsor Protocol Number: MACI00206 | Start Date*: 2008-01-23 | ||||||||||||||||
| Sponsor Name:Genzyme Europe B.V. | ||||||||||||||||||
| Full Title: A Prospective, Randomized, Open-Label, Parallel-Group, Multicenter Study to Demonstrate the Superiority of Matrix-induced Autologous Chondrocyte Implantation (MACI® implant) versus Arthroscopic Mi... | ||||||||||||||||||
| Medical condition: Symptomatic Articular Cartilage Defects of the Femoral Condyle including the Trochlea. osteochondritis dissecans lesions that do not require a bone graft. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) CZ (Completed) SE (Completed) NL (Completed) PL (Completed) DE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-003697-93 | Sponsor Protocol Number: OXITIB2011 | Start Date*: 2011-12-15 | |||||||||||
| Sponsor Name:Hospital Universitario de Canarias | |||||||||||||
| Full Title: Effectiveness of hyperbaric oxygen therapy in the treatment of the open tibial fractures. Open clinical trial, randomized, prospective and controlled. | |||||||||||||
| Medical condition: Open tibial fractures | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004285-34 | Sponsor Protocol Number: STH20370 | Start Date*: 2019-01-18 | |||||||||||
| Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: The impact of aspirin dose modification on the innate immune response - WILL lOWer dose aspirin Therapy ReducE the response to Endotoxin? – (WILLOW TREE) | |||||||||||||
| Medical condition: Acute coronary syndrome | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019415-38 | Sponsor Protocol Number: CZOL446HDE38T | Start Date*: 2011-03-23 | |||||||||||
| Sponsor Name:Universitätsklinikum Würzburg | |||||||||||||
| Full Title: A prospective, bicentric, randomised, primarily double blind, placebo-controlled study to evaluate the efficacy of zoledronic acid for the treatment of bone marrow syndrome | |||||||||||||
| Medical condition: Determination of efficacy of Zoledronic Acid on the treatment of bone marrow edema syndrome. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001556-20 | Sponsor Protocol Number: SB-480848/026 | Start Date*: 2005-11-01 |
| Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
| Full Title: Integrated Biomarker and Imaging Study – 2 (IBIS-2) | ||
| Medical condition: SB-480848 is under developement as a potential anti-atherosclerosis agent for reduction of major cardiovascular events in high risk patient populations. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) CZ (Completed) DE (Completed) AT (Completed) DK (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005763-28 | Sponsor Protocol Number: PM-C-0225 | Start Date*: 2006-10-19 | |||||||||||
| Sponsor Name:Sanofi-Aventis Groupe | |||||||||||||
| Full Title: Randomized, double-blind trial comparing the effects of a 3-month clopidogrel regimen, combined with ASA during the first month, versus ASA alone for the acute treatment of patients with TIA or mi... | |||||||||||||
| Medical condition: the acute treatment of patients with TIA or minor stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Prematurely Ended) ES (Completed) AT (Completed) HU (Prematurely Ended) SK (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004974-16 | Sponsor Protocol Number: IL1ra03 | Start Date*: 2018-11-08 | ||||||||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | ||||||||||||||||||
| Full Title: DOUBLE-BLIND PLACEBO-CONTROLLED RANDOMISED CLINICAL DOSE-RANGING STUDY TREATING MODERATE-SEVERE TRAUMATIC BRAIN INJURY PATIENTS WITH RECOMBINANT HUMAN INTERLEUKIN 1 RECEPTOR ANTAGONIST. | ||||||||||||||||||
| Medical condition: We wish to study the drug Kineret in patients suffering from moderate-to-severe traumatic brain injury | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-002473-21 | Sponsor Protocol Number: ERGCR-18-ORGHIT-001 | Start Date*: 2019-03-05 | |||||||||||
| Sponsor Name:Aspen Global Incorporated | |||||||||||||
| Full Title: An Open-Label, Randomised, Active Controlled, Multi-Centre Phase 3 Study to Evaluate the Safety and Efficacy of Danaparoid vs Argatroban in Treatment of Subjects with Acute HIT (HITSOVA study) | |||||||||||||
| Medical condition: Acute Heparin-induced Thrombocytopenia (HIT) | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) FR (Prematurely Ended) CZ (Prematurely Ended) PL (Completed) ES (Prematurely Ended) HR (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005649-10 | Sponsor Protocol Number: CD-IA-CAM-3001-1107 | Start Date*: 2013-08-19 | |||||||||||
| Sponsor Name:MedImmune Ltd | |||||||||||||
| Full Title: A Phase 2 Exploratory Study of Mavrilimumab versus Anti tumor Necrosis Factor in Subjects with Rheumatoid Arthritis | |||||||||||||
| Medical condition: Rheumatoid arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) PT (Completed) GR (Completed) HU (Completed) CZ (Completed) SK (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001409-40 | Sponsor Protocol Number: S334.2.002 | Start Date*: 2009-03-04 | |||||||||||
| Sponsor Name:Solvay Pharmaceuticals B.V. | |||||||||||||
| Full Title: A Randomized, Double blind, Placebo-Controlled Dose Escalation Study to Investigate the Safety and Pharmacokinetics after Single and Multiple Doses of SLV334 in Sequential Cohorts of Patients with ... | |||||||||||||
| Medical condition: Moderate and severe Traumatic Brain Injury (TBI) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004146-41 | Sponsor Protocol Number: 49RC18_0197 | Start Date*: 2019-01-30 | |||||||||||||||||||||||||||||||
| Sponsor Name:CHU Angers | |||||||||||||||||||||||||||||||||
| Full Title: First-BLINDOS - Evaluation d’une stratégie de dépistage systématique de la carence en vitamine D et du traitement en cas de déficit, sur l’amélioration de la distance maximale de marche chez les pa... | |||||||||||||||||||||||||||||||||
| Medical condition: Artériopathie oblitérante des membres inférieurs de stade 2 | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
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