- Trials with a EudraCT protocol (215)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
215 result(s) found for: SOFA score.
Displaying page 1 of 11.
EudraCT Number: 2012-004819-31 | Sponsor Protocol Number: 1787/12 | Start Date*: 2013-07-08 | |||||||||||
Sponsor Name:RADBOUD UNIVERSITY NIJMEGEN MEDICAL CENTER | |||||||||||||
Full Title: Multicenter open-label RCT to compare colistin alone vs. colistin plus meropenem | |||||||||||||
Medical condition: INFECTIONS DUE TO CARBAPENEM RESISTENT GRAM NEGATIVE BACTERIA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001862-12 | Sponsor Protocol Number: s63213 | Start Date*: 2021-03-23 | ||||||||||||||||
Sponsor Name:University Hospitals Leuven, Clinical Trial Centre | ||||||||||||||||||
Full Title: Early administration of Vitamin C in patients with sepsis or septic shock in emergency departments: a multicentre, double blinded, randomized controlled trial: the C-EASIE trial. | ||||||||||||||||||
Medical condition: We will investigate the potential benefit of early administration of high doses of Vitamin C in addition to standard care in patients with sepsis or septic shock. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001709-10 | Sponsor Protocol Number: P170924J | Start Date*: 2018-10-30 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: I-MICRO: Ilomedine in the treatment of septic shock with persistence of microperfusion disorders: Multicenter randomized and controlled double-blind study. | |||||||||||||
Medical condition: Ilomedin: Cardiology - Angeiology - Vasodilators and anti-ischemic drugs: Severe ischemia: route of injection (Prostaglandin analogs: iloprost) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001766-11 | Sponsor Protocol Number: 2020-24 | Start Date*: 2020-04-29 |
Sponsor Name:ASSISTANCE PUBLIQUE HÔPITAUX DE MARSEILLE | ||
Full Title: Losartan and spironolactone treatment for COVID-19 patients with acute respiratory failure in intensive care unit | ||
Medical condition: Patients with Covid-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
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 (Completed) NL (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014382-12 | Sponsor Protocol Number: IRVASE. | Start Date*: 2009-09-09 |
Sponsor Name:Institut d'Anesthésiologie des Alpes Maritimes | ||
Full Title: ImpImpact du remplissage vasculaire par des solutés équilibrés sur la morbidité des patients de réanimation (IRVASE) : étude randomisée contrôlée monocentrique | ||
Medical condition: Patient de réanimation en état de choc | ||
Disease: | ||
Population Age: | Gender: | |
Trial protocol: FR (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 (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002448-15 | Sponsor Protocol Number: LJ501-CRH01 | Start Date*: 2016-03-18 | |||||||||||
Sponsor Name:La Jolla Pharmaceutical Company, Inc. | |||||||||||||
Full Title: A Phase 3, Placebo-Controlled, Randomized, Double-Blind, Multi-Center Study of LJPC-501 in Patients with Catecholamine-Resistant Hypotension (CRH) | |||||||||||||
Medical condition: Catecholamine-Resistant Hypotension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) FI (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003942-35 | Sponsor Protocol Number: APHP200018 | Start Date*: 2021-04-27 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux Paris | |||||||||||||
Full Title: HydrOcortisone and fludRocortisoNe for critical ILLness-related corticosteroid insufficiency | |||||||||||||
Medical condition: Critically ill patients with a SOFA score (SOFA; Sequential Organ Failure Assessment) ≥ 6, for at least 6 consecutive hours, suffering from CIRCI, to the notable exception of patients with septic s... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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 (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004123-67 | Sponsor Protocol Number: PHRCI2012/CHOCMSC-GIBOT/SKJ | Start Date*: 2021-04-30 |
Sponsor Name:Centre Hospitalier Régional Universitaire de Nancy | ||
Full Title: CHOCMSC Study Effects of mesenchymal stem cells administration on organ failure during septic shock: Phase II randomized placebo-controlled study | ||
Medical condition: septic shock | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004108-16 | Sponsor Protocol Number: HOFATA_v3.0 | Start Date*: 2022-04-21 |
Sponsor Name:Medical University Vienna | ||
Full Title: Host factors predicting target site concentration of antibiotics in critically ill patients: An explorative pharmacokinetic biomarker study | ||
Medical condition: All patients given standard of care intravenous therapy of the studied antibiotics will be screened against the inclusion criteria. Two groups are included: Group A (septic patients with organ dysf... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000136-17 | Sponsor Protocol Number: Target_ZKSJ0085 | Start Date*: 2016-08-22 |
Sponsor Name:Friedrich Schiller University Jena | ||
Full Title: Prospective, randomized, multicenter clinical trial on the impact of Therapeutic Drug Monitoring (TDM) of piperacillin on organ functions and survival in the treatment of severe sepsis or septic shock | ||
Medical condition: Patients with a severe sepsis oder a septic shock treatet with piperacillin/tazobactam | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004674-49 | Sponsor Protocol Number: LEVOHLM | Start Date*: 2007-12-28 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: Levosimendan vor Herz-Lungen-Maschine bei Coronary artery bypass graft-Operationen | ||
Medical condition: The drug Levosimendan / Simdax (R) will be investigated in patients undergoing coronary artery bypass graft operations. The study population will be patients with impaired myocardial function as st... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-004827-36 | Sponsor Protocol Number: MOT-C-203 | Start Date*: 2019-08-07 | |||||||||||
Sponsor Name:INOTREM S.A. | |||||||||||||
Full Title: Efficacy, Safety and Tolerability of Nangibotide in Patients with Septic Shock. A Randomized, Double-blind, Placebo Controlled Dose Selection Study. | |||||||||||||
Medical condition: Septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) ES (Ongoing) DK (Completed) FI (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001206-35 | Sponsor Protocol Number: ACEI-COVID-19 | Start Date*: 2020-04-14 |
Sponsor Name:Medizinische Universität Innsbruck | ||
Full Title: Stopping ACE-inhibitors in COVID-19 - a randomized, controlled clinical trial | ||
Medical condition: The study will investigate infections with the new SARS-CoV2 virus. Current studies show that the SARS-CoV2 virus penetrates human cells via the angiotensin converting enzyme II (ACE2) receptor 2. ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005761-19 | Sponsor Protocol Number: P060213 | Start Date*: 2007-03-09 |
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
Full Title: Ketamine versus etomidate au cours de l'intubation en séquence rapide : conséquences sur la morbidité hospitalière | ||
Medical condition: Patients adultes présentant une activité cardiaque spontanée nécesitant une intubation endotrachéale, pris en charge par les SMUR et les SAMU participants. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000488-98 | Sponsor Protocol Number: PPI-SepsisTrial | Start Date*: 2018-07-12 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: Proton pump inhibitors (PPI) as a new strategy for therapy in sepsis: clinical trial to reduce severity of organ failure and in vitro experiments to search specific hallmarks in monocytes from sept... | |||||||||||||
Medical condition: Sepsis is a severe disease with a high mortality rate and lack of efficacious therapies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001582-16 | Sponsor Protocol Number: RF-2016-02361583 | Start Date*: 2018-08-09 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO | |||||||||||||
Full Title: Efficacy of Albumin Replacement and Balanced Crystalloid Solutions in Septic Shock (the ALBIOSS-BALANCED trial): a 2-by-2 factorial, investigator-initiated, open-label, multicenter, randomized, con... | |||||||||||||
Medical condition: Septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001336-10 | Sponsor Protocol Number: AGNES-19 | Start Date*: 2022-03-25 | |||||||||||
Sponsor Name:University Medical Centre Hamburg-Eppendorf | |||||||||||||
Full Title: Multicenter, randomized, double-blind, biomarker-guided, phase II trial with Adrecizumab (HAM 8101) to improve proGNosis and outcomES in patients with moderate to severe covid-19 - Adrecizumab (HAM... | |||||||||||||
Medical condition: COVID-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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