- Trials with a EudraCT protocol (77)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
77 result(s) found for: Transfusion Reactions.
Displaying page 1 of 4.
EudraCT Number: 2012-002920-33 | Sponsor Protocol Number: CLI00076 | Start Date*: 2012-12-10 |
Sponsor Name:CERUS CORPORATION | ||
Full Title: A Randomized Controlled Study to Evaluate Efficacy and Safety of S-303 Treated Red Blood Cells in Subjects with Thalassemia Major Requiring Chronic RBC Transfusion | ||
Medical condition: Subjects with Thalassemia Major Requiring Chronic RBC Transfusion | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002622-39 | Sponsor Protocol Number: PEDFOI | Start Date*: 2015-11-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | |||||||||||||
Full Title: Experimental Study Protocol on Treatment with plasma transfusions in Patients affected by type VI Osteogenesis Imperfecta | |||||||||||||
Medical condition: type VI Osteogenesis Imperfecta | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000936-24 | Sponsor Protocol Number: SHINE-TRAUMA | Start Date*: 2019-05-02 | |||||||||||
Sponsor Name:Section for Transfusion Medicine, Capital Region Blood Bank, Copenhagen University Hospital | |||||||||||||
Full Title: Efficacy and safety of 72-hour infusion of Prostacyclin (1 ng/kg/min) in trauma patients with haemorrhagic shock induced endotheliopathy – a multicentre randomized, placebo-controlled, blinded, inv... | |||||||||||||
Medical condition: Shock-induced endotheliopathy in trauma patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003173-28 | Sponsor Protocol Number: 11112 | Start Date*: 2012-06-13 |
Sponsor Name:Helsinki University Hospital | ||
Full Title: Volume replacement therapy in cardiac surgery: effect on renal function. | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001867-22 | Sponsor Protocol Number: PRETIC | Start Date*: 2018-09-27 | |||||||||||
Sponsor Name:Banc de Sang i teixits | |||||||||||||
Full Title: TRANSFUSION OF RED BLOOD CELLS, TRANEXAMIC ACID AND FIBRINOGEN CONCENTRATE FOR SEVERE TRAUMA HEMORRHAGE AT PRE-HOSPITAL PHASE OF CARE. A PILOT TRIAL. | |||||||||||||
Medical condition: TREATMENT OF SEVERE TRAUMA HEMORRHAGE AT PRE-HOSPITAL PHASE OF CARE. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003978-16 | Sponsor Protocol Number: PRooF-iTH | Start Date*: 2015-01-22 | ||||||||||||||||
Sponsor Name:Section for Transfusion Medicine, Capitol Region Blood Bank | ||||||||||||||||||
Full Title: Pilot Randomized trial of Fibrinogen in Trauma Haemorrhage (PRooF-iTH). | ||||||||||||||||||
Medical condition: Trauma patients with ongoing haemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001296-33 | Sponsor Protocol Number: COMBAT-COVID-19 | Start Date*: 2020-05-06 | ||||||||||||||||
Sponsor Name:Section for Transfusion Medicine, Capital Region Blood bank, Copenhagen University Hospital | ||||||||||||||||||
Full Title: Efficacy and safety of 72-hour infusion of Prostacyclin (1 ng/kg/min) in patients with COVID-19 induced respiratory failure – a multicentre randomized, placebo-controlled, blinded, investigator-ini... | ||||||||||||||||||
Medical condition: COVID-19 induced respiratory failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002341-20 | Sponsor Protocol Number: PLAF1003 | Start Date*: 2008-07-10 |
Sponsor Name:Queen Charlotte's and Chelsea Hospital | ||
Full Title: Randomized controlled trial comparing the effect of carbetocin vs syntocinon and ergometrine on postpartum haemorrhage in patients undergoing elective caesarean section | ||
Medical condition: Clinical efficacy comparing ( 2 drugs) carbetocin Vs syntocinon and ergometrine | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003416-38 | Sponsor Protocol Number: TMP-0916_02 | Start Date*: 2018-04-05 | |||||||||||
Sponsor Name:Fraunhofer Gesellschaft for its Institute Fraunhofer Institute for Molecular Biology and Applied Ecology (IME) | |||||||||||||
Full Title: Randomised, open lable, active controlled clinical trial to demonstrate safety and efficacy of an i.v. administration of Polyglucoferron compared to i.v. Ferric Carboxymaltose and oral iron substit... | |||||||||||||
Medical condition: preoperative iron deficiency anaemia in patients with planned elective non-cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001829-11 | Sponsor Protocol Number: UoL001337 | Start Date*: 2018-10-04 | |||||||||||
Sponsor Name:University of Liverpool | |||||||||||||
Full Title: The Carboprost or Oxytocin Postpartum haemorrhage Effectiveness Study. Carboprost vs Oxytocin as the First Line Treatment of Primary Postpartum Haemorrhage; A phase IV, double-blind, double-dummy, ... | |||||||||||||
Medical condition: Primary postpartum haemorrhage | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003235-30 | Sponsor Protocol Number: H9H-MC-JBAV | Start Date*: 2014-02-10 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Phase 2/3 Study of Monotherapy LY2157299 Monohydrate in Very Low-, Low-, and Intermediate-Risk Patients with Myelodysplastic Syndromes | |||||||||||||
Medical condition: Myelodysplastic Syndromes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005486-14 | Sponsor Protocol Number: EPIC-19 | Start Date*: 2021-01-11 |
Sponsor Name:Wroclaw Medical University | ||
Full Title: Using of convalescent plasma in the treatment of COVID-19 patients with metabolomic and laboratory evaluation of the progress of plasma therapy | ||
Medical condition: Covid-19 (Coronavirus Disease 2019) – acute infectious disease of the respiratory system caused by SARS-CoV-2 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-000568-32 | Sponsor Protocol Number: CLLTX1 | Start Date*: 2017-11-07 | ||||||||||||||||
Sponsor Name:Universität Köln | ||||||||||||||||||
Full Title: Obinutuzumab containing conditioning regimen for CLL patients and patients with Richter`s transformation requiring an allogeneic stem cell transplantation | ||||||||||||||||||
Medical condition: Patients with poor risk CLL and Richter`s transformation requiring an allogeneic stem cell transplantation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004931-21 | Sponsor Protocol Number: BO42162 | Start Date*: 2020-10-26 | |||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||
Full Title: A PHASE III, RANDOMIZED, OPEN-LABEL, ACTIVE-CONTROLLED, MULTICENTER STUDY EVALUATING THE EFFICACY AND SAFETY OF CROVALIMAB VERSUS ECULIZUMAB IN ADULT AND ADOLESCENT PATIENTS WITH PAROXYSMAL NOCTUR... | |||||||||||||
Medical condition: Paroxysmal Nocturnal Hemoglobinuria (PNH) | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) DE (Ongoing) HU (Completed) FR (Ongoing) PL (Ongoing) GR (Completed) PT (Ongoing) BE (Ongoing) IE (Prematurely Ended) EE (Completed) LT (Ongoing) IT (Prematurely Ended) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003122-28 | Sponsor Protocol Number: ArgLepi-2006 | Start Date*: 2008-12-19 | |||||||||||
Sponsor Name:Heinrich-Heine-Universität Düsseldorf | |||||||||||||
Full Title: Argatroban versus Lepirudin in Critically Ill Patients | |||||||||||||
Medical condition: Critically ill patients are usually treated with heparin for anticoagulation. A serious complication of heparin therapy is heparin-induced thrombocytopenia type II (HIT). Patients with HIT have t... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003439-12 | Sponsor Protocol Number: TMP-0916_03 | Start Date*: 2018-02-19 | |||||||||||
Sponsor Name:Fraunhofer Gesellschaft for its Institute Fraunhofer für Translationale Medizin und Pharmakologie (ITMP) | |||||||||||||
Full Title: Safety and efficacy of postoperative i.v. iron substitution with Polyglucoferron compared to Ferric Carboxymaltose and oral iron in patients with diagnosed iron deficiency who develop anaemia pre- ... | |||||||||||||
Medical condition: pre-operative iron deficiency in patients with planned elective surgery and pre-/post-operative iron deficiency anamia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004677-20 | Sponsor Protocol Number: Gemtax IV | Start Date*: 2006-03-17 |
Sponsor Name:University of Heidelberg, Klinikum Mannheim, Dep Surgery/Thoracical Oncology | ||
Full Title: Randomised Phase II/III Study on Sectional Single Agent Gemcitabine and Docetaxel Versus Carboplatine / Gemcitabine Doublet Therapy, both combined Cetuximab in the Treatment of Advanced NSCLC (Stag... | ||
Medical condition: Lung cancer remains the leading cause of cancer-related death in men and has increased its incidence in women over the past decades (protocol page 9). Data from both meta-analysis and clinical tria... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000452-28 | Sponsor Protocol Number: VIPER-OCTA | Start Date*: 2014-11-05 | |||||||||||
Sponsor Name:Section for Transfusion Medicine, Capitol Region Blood Bank | |||||||||||||
Full Title: Vasculopathic Injury and Plasma as Endothelial Rescue – OCTAplas trial | |||||||||||||
Medical condition: patients undergoing emergency surgery for thoracic aortic dissections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019224-31 | Sponsor Protocol Number: IGR2009/1593 | Start Date*: 2012-06-06 | |||||||||||||||||||||
Sponsor Name:Institut Gustave Roussy | |||||||||||||||||||||||
Full Title: INTERGROUP TRIAL FOR CHILDREN OR ADOLESCENTS WITH B-CELL NHL OR B-AL: EVALUATION OF RITUXIMAB EFFICACY AND SAFETY IN HIGH RISK PATIENTS | |||||||||||||||||||||||
Medical condition: untreated advanced stage B-cell NHL or B-AL. | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Ongoing) GB (GB - no longer in EU/EEA) FR (Completed) ES (Temporarily Halted) NL (Completed) HU (Ongoing) IT (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001923-53 | Sponsor Protocol Number: 7980 | Start Date*: 2015-10-07 | |||||||||||
Sponsor Name:Rafael Bielza Galindo | |||||||||||||
Full Title: Intravenous iron, early functional recovery and delirium in patients atients with hip fracture | |||||||||||||
Medical condition: Hip fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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