- Trials with a EudraCT protocol (179)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
179 result(s) found for: bacterial infections and sepsis.
Displaying page 1 of 9.
EudraCT Number: 2011-005902-30 | Sponsor Protocol Number: FAR01-2011 | Start Date*: 2012-02-13 | ||||||||||||||||
Sponsor Name:Servicio de Farmacia. Hospital Universitari de Bellvitge | ||||||||||||||||||
Full Title: | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002788-28 | Sponsor Protocol Number: RHM CHI434 | Start Date*: 2008-01-15 | ||||||||||||||||
Sponsor Name:Southampton University Hospital NHS Trust | ||||||||||||||||||
Full Title: Evaluation of Corticosteroid therapy in Childhood Severe Sepsis (Steroids in Paediatric Sepsis, StePS) - a randomised pilot study | ||||||||||||||||||
Medical condition: Children with severe sepsis requiring mechanical ventilation presenting within 12 hours of onset. The majority of children will either have community acquired sepsis (most commonly meningococcal or... | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000717-24 | Sponsor Protocol Number: 230390 | Start Date*: 2017-08-24 | |||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
Full Title: Concentration of piperacillin in plasma and subcutis in patients on crrt treatment | |||||||||||||||||||||||
Medical condition: infections reloated to CRRT | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002926-35 | Sponsor Protocol Number: 080716CT | Start Date*: 2017-01-16 | |||||||||||
Sponsor Name:Alder Hey Children's Foundation NHS Trust | |||||||||||||
Full Title: Pharmacokinetics of post-operative Cefuroxime in infants undergoing cardiac surgery | |||||||||||||
Medical condition: post operative paediatric cardiac patients | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011346-26 | Sponsor Protocol Number: MAB-N007 | Start Date*: 2009-11-27 | ||||||||||||||||
Sponsor Name:Biosynexus Incorporated | ||||||||||||||||||
Full Title: Ensayo de fase 2b/3, multicéntrico, aleatorizado, doble ciego, controlado con placebo, para evaluar la seguridad y eficacia de Pagibaximab Inyectable en recién nacidos con peso de nacimiento muy ba... | ||||||||||||||||||
Medical condition: Prevención de la septicemia causada por estafilococos en recién nacidos con peso de nacimiento muy bajo. | ||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) GB (Completed) DE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001019-95 | Sponsor Protocol Number: COLIMICINA | Start Date*: 2021-05-31 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Pharmacokinetic/pharmacodynamic aspects of colistin intravenous administration in critically ill patients suffering from hospital infections caused by multi-antibiotic-resistant germs and receiving... | |||||||||||||
Medical condition: Critically ill patients suffering from hospital infections caused by multi-antibiotic-resistant germs and receiving continuous renal replacement therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001056-55 | Sponsor Protocol Number: INCLASS | Start Date*: 2017-08-28 | |||||||||||
Sponsor Name:HELLENIC INSTITUTE FOR THE STUDY OF SEPSIS | |||||||||||||
Full Title: A DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED CLINICAL STUDY OF THE EFFICACY OF INTRAVENOUS CLARITHROMYCIN AS ADJUNCTIVE TREATMENT IN PATIENTS WITH SEPSIS AND RESPIRATORY AND MULTIPLE ORGAN DYSFUN... | |||||||||||||
Medical condition: IMMUNE MODULATION WITH CLARITHROMYCIN IN SEPSIS WITH MULTIPLE ORGAN AND RESPIRATORY DYSFUNCTION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Ongoing) BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003698-13 | Sponsor Protocol Number: ABR-54775 | Start Date*: 2015-12-30 | |||||||||||
Sponsor Name:Radboudumc | |||||||||||||
Full Title: Neuroinflammation in sepsis encephalopathy: the NINEVEH-study | |||||||||||||
Medical condition: sepsis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002555-26 | Sponsor Protocol Number: RH-RBWH-2014-1 | Start Date*: 2014-07-25 | |||||||||||
Sponsor Name:Dept. of Intensive Care Medicine, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: MEROPENEM and CIPROFLOXACIN DOSING IN THE CRITICALLY ILL PATIENT WITH SEPTIC SHOCK – A SINGLE CENTER PHARMACOKINETIC STUDY | |||||||||||||
Medical condition: Septic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005768-74 | Sponsor Protocol Number: ImmunoSep | Start Date*: 2021-02-18 | |||||||||||
Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
Full Title: PERSONALIZED IMMUNOTHERAPY IN SEPSIS: A MULTICENTRE AND MULTINATIONAL, DOUBLE-BLIND, DOUBLE-DUMMY RANDOMIZED CLINICAL TRIAL (THE IMMUNOSEP TRIAL) | |||||||||||||
Medical condition: Sepsis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Ongoing) NL (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004333-42 | Sponsor Protocol Number: SISPCT | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Friedrich-Schiller-University of Jena | |||||||||||||
Full Title: Prospective randomized clinical multicenter trial about the effect of an adjunctive intravenous treatment with sodium selenite (selenase®T, double-blind) and a procalcitonin guided causal therapy (... | |||||||||||||
Medical condition: severe sepsis / septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002251-42 | Sponsor Protocol Number: 3-001 | Start Date*: 2012-11-05 | |||||||||||
Sponsor Name: Asahi Kasei Pharma America Corporation | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE BLIND, PLACEBO–CONTROLLED, PHASE 3 STUDY TO ASSESS THE SAFETY AND EFFICACY OF ART-123 IN SUBJECTS WITH SEVERE SEPSIS AND COAGULOPATHY | |||||||||||||
Medical condition: severe sepsis and coagulopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) HU (Completed) FI (Completed) CZ (Completed) ES (Completed) BG (Prematurely Ended) GB (Completed) DE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002171-26 | Sponsor Protocol Number: PROVIDE | Start Date*: 2017-10-20 | |||||||||||
Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
Full Title: A PERSONALIZED RANDOMIZED TRIAL OF VALIdATION AND RESTORATION OF IMMUNE DYSFUNCTION IN SEVERE INFECTIONS AND SEPSIS: THE PROVIDE TRIAL | |||||||||||||
Medical condition: A TRIAL FOR IMMUNOMODULATION IN SEPSIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000902-37 | Sponsor Protocol Number: RH-ITA-005 | Start Date*: 2014-06-27 | |||||||||||
Sponsor Name:Dept. of Intensive Care, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: Conservative vs. Liberal Approach to fluid therapy of Septic Shock in Intensive Care | |||||||||||||
Medical condition: Septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004834-32 | Sponsor Protocol Number: PROTEINA-C | Start Date*: 2012-06-08 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: Administration of concentrated Protein C in patients with severe sepsis and contraindications to activated protein C. A monocentric, randomised placebo-controlled study. | |||||||||||||
Medical condition: patients affected by severe sepsis admitted to intensive care | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015168-32 | Sponsor Protocol Number: D0620C00003 | Start Date*: 2010-10-04 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multicentre, Randomised, Double Blind, Placebo controlled Phase IIb Study to compare the Efficacy and Safety of Two Dosing Regimens of Intravenous Infusions of CytoFab™ (AZD9773) in Adult Patient... | |||||||||||||
Medical condition: Severe sepsis and/or septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) ES (Completed) CZ (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002840-42 | Sponsor Protocol Number: 3/035/14 | Start Date*: 2014-12-15 | |||||||||||
Sponsor Name:University of Aberdeen [...] | |||||||||||||
Full Title: Dose assessment of melatonin in sepsis trial (DAMSEL 2) | |||||||||||||
Medical condition: Sepsis | |||||||||||||
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Population Age: Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002011-33 | Sponsor Protocol Number: PROGRESS | Start Date*: 2017-08-28 | |||||||||||
Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
Full Title: A RANDOMIZED PROSPECTIVE CLINICAL TRIAL TO ASSESS THE ROLE OF PROCALCITONIN-GUIDED ANTIMICROBIAL THERAPY TO REDUCE LONG-TERM INFECTIONS SEQUELAE | |||||||||||||
Medical condition: USE OF PROCALCITONIN IN EARLY STOP OF ANTIBIOTICS TO AVOID LONG-TERM CONSEQUENCES | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001008-13 | Sponsor Protocol Number: SUPERIOR | Start Date*: 2018-07-09 | |||||||||||
Sponsor Name:HELLENIC INSTITUTE FOR THE STUDY OF SEPSIS | |||||||||||||
Full Title: A SUPAR GUIDED DOUBLE BLIND RANDOMIZED CLINICAL TRIAL OF INITIATION OF ANTIBIOTICS FOR PRESUMED INFECTION AT THE EMERGENCY DEPARTMENT: THE SUPERIOR TRIAL | |||||||||||||
Medical condition: Α suPAR guided early antibiotic administration at the Emergency Room for presumed infection and sepsis and evaluation of the impact of this intervention to the patients’ final outcome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004239-29 | Sponsor Protocol Number: E2011OBINFECTION | Start Date*: 2011-10-04 | |||||||||||
Sponsor Name:Hopital Erasme | |||||||||||||
Full Title: what are the optimal doses of broad spectrum B-lactams to administer to obese patients if infected? | |||||||||||||
Medical condition: any patient with a BMI >= 30kg/m² and has a simple or severe infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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