- Trials with a EudraCT protocol (122)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
122 result(s) found for: Multiple organ failure.
Displaying page 1 of 7.
| EudraCT Number: 2012-005159-18 | Sponsor Protocol Number: CRO2047 | Start Date*: 2013-08-28 | ||||||||||||||||
| Sponsor Name:Imperial College, London | ||||||||||||||||||
| Full Title: An efficacy and mechanism evaluation study of Levosimendan for the Prevention of Acute oRgan Dysfunction in Sepsis (LeoPARDS) | ||||||||||||||||||
| Medical condition: Septic shock. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-002547-94 | Sponsor Protocol Number: 2011-420 | Start Date*: 2013-03-25 | ||||||||||||||||
| Sponsor Name:Dept. of Intensive Care 4131, Rigshospitalet | ||||||||||||||||||
| Full Title: Early Goal-Directed Nutrition in ICU Patients – EAT-ICU Trial | ||||||||||||||||||
| Medical condition: Acutely admitted, mechanically ventilated intensive care unit patients. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2007-004856-35 | Sponsor Protocol Number: DHTCA_P09889 | Start Date*: 2008-03-17 | ||||||||||||||||||||||||||
| Sponsor Name:Imperial College London | ||||||||||||||||||||||||||||
| Full Title: Scavenging free haemoglobin atenuates the systemic inflmmatory response following surgery | ||||||||||||||||||||||||||||
| Medical condition: Systemic inflammatory response and associated multiorgan failure that follows cardiopulmonary bypass for cardiac surgery | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-002255-10 | Sponsor Protocol Number: IRMINEpilot | Start Date*: 2016-06-30 | ||||||||||||||||||||||||||
| Sponsor Name:Abertawe Bro Morgannwg University Health Board | ||||||||||||||||||||||||||||
| Full Title: INFLAMMATORY RESPONSE IN MAJOR INJURY & RECOMBINANT HUMAN ERYTHROPOIETIN (IRMINE) - A PILOT STUDY | ||||||||||||||||||||||||||||
| Medical condition: Post-trauma multiple organ failure: a manifestation of the systemic inflammatory/immune response to major injuries. | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-000899-25 | Sponsor Protocol Number: FP1CLI006 | Start Date*: 2016-12-16 | |||||||||||
| Sponsor Name:Faron Pharmaceuticals Ltd | |||||||||||||
| Full Title: A Phase II Double-blind, Randomised, Parallel Group 2:1 Comparison of the Efficacy and Safety of FP-1201-lyo (Recombinant Human Interferon Beta-1a) and Placebo in the Prevention of Multi-Organ Fail... | |||||||||||||
| Medical condition: Prevention of Multi-Organ Failure on Patients Surviving Open Surgery for a Ruptured Abdominal Aortic Aneurysm. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) EE (Prematurely Ended) LT (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004886-33 | Sponsor Protocol Number: A06-269 | Start Date*: 2007-06-05 |
| Sponsor Name:University of Athens, Medical school | ||
| Full Title: A DOUBLE-BLIND RANDOMIZED PLACEBO-CONTROLLED CLINICAL TRIAL OF THE SAFETY AND IMMUNOMODULATORY THERAPY FOR THE MANAGEMENT OF SEPSIS | ||
| Medical condition: septic syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-021557-40 | Sponsor Protocol Number: MM-Rel | Start Date*: 2011-03-03 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: A phase III trial comparing bortezomib, cyclophosphamide and dexamethasone versus lenalinomide cyclophosphamide and dexamethasone in patients with multiple myeloma at first relapse | |||||||||||||
| Medical condition: Multiple mieloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004884-29 | Sponsor Protocol Number: 12-BI-505-02 | Start Date*: 2013-01-16 | |||||||||||
| Sponsor Name:BioInvent International AB | |||||||||||||
| Full Title: A single-arm, Open-label, Phase 2 Clinical Trial Evaluating Disease Response Following Treatment With BI-505, a Human Anti–Intercellular Adhesion Molecule 1 Monoclonal Antibody, In Patients With Sm... | |||||||||||||
| Medical condition: Smoldering (asymptomatic) multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-016871-32 | Sponsor Protocol Number: 0911001 | Start Date*: 2010-06-28 | ||||||||||||||||
| Sponsor Name:CHU de TOULOUSE | ||||||||||||||||||
| Full Title: A Randomized Phase III Study Comparing Conventional Dose Treatment Using a Combination of Lenalidomide, Bortezomib and Dexamethasone (RVD) to High-Dose Treatment with Peripheral Stem Cell Transplan... | ||||||||||||||||||
| Medical condition: Myeloma, Multiple Myeloma | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) BE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-001594-31 | Sponsor Protocol Number: 2022_0174 | Start Date*: 2022-08-30 | |||||||||||
| Sponsor Name:CHU de LILLE | |||||||||||||
| Full Title: A Phase 2 Study of Teclistamab in Combination with Daratumumab or Lenalidomide in Elderly Patients with Newly Diagnosed Multiple Myeloma | |||||||||||||
| Medical condition: A Phase 2 Study of Teclistamab in Combination with Daratumumab or Lenalidomide in Elderly Patients with Newly Diagnosed Multiple Myeloma | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000301-40 | Sponsor Protocol Number: 009531 | Start Date*: 2016-03-11 |
| Sponsor Name:Queen Mary University of London | ||
| Full Title: A randomised, blinded, placebo-controlled Phase 2a study to evaluate the safety and efficacy of Artesunate treatment in severely injured trauma patients with traumatic haemorrhage. | ||
| Medical condition: Organ Dysfunction and Failure in Traumatic Hemorrhage | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-003023-38 | Sponsor Protocol Number: GERMAIN | Start Date*: 2013-10-30 | |||||||||||
| Sponsor Name:Friedrich-Schiller-Universität Jena | |||||||||||||
| Full Title: Phase II study of Bortezomib, Melphalan, Prednisone (VMP) followed by Lenalidomide maintenance vs. VMP without maintenance in Myeloma patients not eligible to high-dose chemotherapy and autologous ... | |||||||||||||
| Medical condition: multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001100-38 | Sponsor Protocol Number: FARM97AJNN | Start Date*: 2014-07-09 | |||||||||||
| Sponsor Name:DIPART. DI NEUROSCIENZE, SCIENZE RIPRODUTTIVE E ODONTOSTOMATOLOGICHE DELL’UNIVERSITà DEGLI STUDI DI NAPOLI “FEDERICO II" | |||||||||||||
| Full Title: Antagonists of Angiotensin II Receptors in sepsis | |||||||||||||
| Medical condition: SEPSIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002120-24 | Sponsor Protocol Number: OP-104 | Start Date*: 2017-12-14 | |||||||||||
| Sponsor Name:Oncopeptides AB | |||||||||||||
| Full Title: An Open-Label Phase 1/2a Study of the Safety and Efficacy of Melflufen and Dexamethasone in Combination with either Bortezomib or Daratumumab in Patients with Relapsed or Relapsed-Refractory Multip... | |||||||||||||
| Medical condition: Patients with Relapsed or Relapsed-Refractory Multiple Myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) ES (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000654-22 | Sponsor Protocol Number: 6998 | Start Date*: 2018-11-09 |
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
| Full Title: A Prospective, Randomized Multicenter, Double Blind Clinical Trial Comparing Inhaled Dornase Alfa and Its Placebo to Reduce the Incidence of Moderate to Severe ARDS in Ventilated Trauma Patients in... | ||
| Medical condition: Multiple Trauma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-006782-83 | Sponsor Protocol Number: EC08/00230 | Start Date*: 2013-09-24 |
| Sponsor Name:Hospital Universitario Virgen de las Nieves | ||
| Full Title: Prevention MODS by modulating the inflammatory response through melatonin administration in surgical patients with severe sepsis. | ||
| Medical condition: Septic patients of abdominal surgery | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004810-25 | Sponsor Protocol Number: 205678 | Start Date*: 2018-07-19 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A Phase II, Open Label, Randomized, Two-Arm Study to Investigate the Efficacy and Safety of Two Doses of the Antibody Drug Conjugate GSK2857916 in Participants with Multiple Myeloma Who Had 3 or Mo... | |||||||||||||
| Medical condition: Relapsed/Refractory Multiple Myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004689-93 | Sponsor Protocol Number: 207497 | Start Date*: 2019-04-29 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A Phase I/II, Open-label, Dose Escalation and Expansion Study to Evaluate Safety, Tolerability, and Clinical Activity of the Antibody-Drug Conjugate GSK2857916 Administered in Combination with Lena... | |||||||||||||
| Medical condition: Relapsed / Refractory Multiple Myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002112-99 | Sponsor Protocol Number: F1K-MC-EVDK | Start Date*: 2006-09-26 | |||||||||||
| Sponsor Name:Eli Lilly & Company Limited | |||||||||||||
| Full Title: A Phase 2 Study to Evaluate Dose and Duration of Treatment of Drotrecogin Alfa (Activated) Using Serial Measurements of Protein C in Patients with Severe Sepsis and Multiple Organ Dysfunction | |||||||||||||
| Medical condition: severe sepsis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) SE (Prematurely Ended) FR (Completed) FI (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003993-29 | Sponsor Protocol Number: 207503 | Start Date*: 2020-05-12 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: DREAMM 7: A Multicenter, Open-Label, Randomized Phase III Study to Evaluate the Efficacy and Safety of the Combination of Belantamab Mafodotin, Bortezomib, and Dexamethasone (B-Vd) Compared with th... | |||||||||||||
| Medical condition: Relapsed/Refractory Multiple Myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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