- Trials with a EudraCT protocol (2,333)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
2,333 result(s) found for: Mortality.
Displaying page 1 of 117.
EudraCT Number: 2012-002235-29 | Sponsor Protocol Number: 1.0 | Start Date*: 2012-10-23 |
Sponsor Name:Medizinische Universität Wien - Universitätsklinik für klinische Pharmakologie | ||
Full Title: Does acetylsalicylic acid reduce the mortality of patients admitted to an Intensive Care Unit | ||
Medical condition: medical patients admitted to an intensive care unit | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-000497-38 | Sponsor Protocol Number: DEX-PCH-VMNI | Start Date*: 2016-08-23 |
Sponsor Name:Ana Vallejo De la Cueva | ||
Full Title: Dexmedetomidine versus current clinical practice for non-invasive mechanical ventilation: a randomized clinical trial | ||
Medical condition: Accute respiratory insuffienciency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
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: 2010-024263-40 | Sponsor Protocol Number: PEx in DIC Version 1 | Start Date*: 2011-09-08 |
Sponsor Name:Medizinische Universität Wien, Univ. Klinik f. Klinische Pharmakologie | ||
Full Title: Plasma exchange as therapy for disseminated intrevascular coagulation (DIC)- a randomized-controlled trial | ||
Medical condition: Disseminated intravascular coagulation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-001333-13 | Sponsor Protocol Number: 20-37815010 | Start Date*: 2020-04-09 |
Sponsor Name:Groupe Hospitalier Paris Saint-Joseph | ||
Full Title: Dexamethasone associated with hydroxychloroquine vs. hydroxychloroquine alone for the early treatment of severe ARDS caused by COVID-19 : a randomized controlled trial | ||
Medical condition: Acute Respiratory Distress Syndrome (ARDS) caused by SARS-Cov-2 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
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: 2022-003218-36 | Sponsor Protocol Number: 82646 | Start Date*: 2023-06-05 |
Sponsor Name:Radboudumc | ||
Full Title: The safety of ticagrelor monotherapy after primary percutaneous coronary intervention for ST-elevation myocardial infarction and the effect on intramyocardial haemorrhage | ||
Medical condition: Acute myocardial infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005533-20 | Sponsor Protocol Number: VOLATILE10600 | Start Date*: 2014-12-11 |
Sponsor Name:OSPEDALE SAN RAFFAELE IRCCS | ||
Full Title: VOLATILE ANESTHETICS TO REDUCE MORTALITY IN CARDIAC SURGERY. A MULTICENTRE RANDOMIZED CONTROLLER STUDY | ||
Medical condition: PATIENTS UNDERGOING CORONARY ARTERY BYOASS GRAFT SURGERY | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001479-22 | Sponsor Protocol Number: NCT03021525 | Start Date*: 2017-08-04 |
Sponsor Name:University Medical Center Hamburg-Eppendorf, Germany | ||
Full Title: Individualized perioperative hemodynamic goal-directed therapy in major abdominal surgery (iPEGASUS-trial) | ||
Medical condition: - Hemodynamic Instability - Cardiac Output - High Peroperative Complication | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001250-21 | Sponsor Protocol Number: 2020/3078 | Start Date*: 2020-04-03 |
Sponsor Name:GUSTAVE ROUSSY | ||
Full Title: COVID-19 - Epidemiology of SARS-CoV-2 and Mortality to Covid19 Disease upon Hydroxychloroquine and Azithromycin Therapy in French Cancer patients | ||
Medical condition: Patients eligible for, or under, or recently treated by chemotherapy (CT) and/or immune-checkpoint blockade (ICB) for the treatment of solid tumors or hematological malignancies. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000436-74 | Sponsor Protocol Number: 432 | Start Date*: 2007-11-27 | |||||||||||
Sponsor Name:Poissy Hospital | |||||||||||||
Full Title: Impact of two glucose control regimens by insulin on hospital mortality in intensive care unit patients (INSUREA Study) | |||||||||||||
Medical condition: hyperglycemia in critical care unit patients | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003539-56 | Sponsor Protocol Number: 1.01 | Start Date*: 2006-11-10 |
Sponsor Name:Medical University of Vienna, Department of Internal Medicine IV | ||
Full Title: Simvastatin in patients with septic shock | ||
Medical condition: Septic shock | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001099-21 | Sponsor Protocol Number: 2010-04-23 | Start Date*: 2011-05-19 |
Sponsor Name:Population Health Research Institute | ||
Full Title: SIRS Steroids In caRdiac Surgery Trial | ||
Medical condition: From available evidence, corticosteroids attenuate the inflammatory response to CPB which is felt to contribute to morbidity and mortality in cardiac surgery patients. The meta-analysis of the lite... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003510-16 | Sponsor Protocol Number: EFC15156 | Start Date*: 2018-05-07 | ||||||||||||||||
Sponsor Name:Lexicon Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Effects of Sotagliflozin on Clinical Outcomes in Hemodynamically Stable Patients with Type 2 Diabet... | ||||||||||||||||||
Medical condition: Cardiovascular diseases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) NL (Completed) ES (Prematurely Ended) LV (Completed) LT (Completed) GB (Completed) BE (Completed) DK (Prematurely Ended) FR (Completed) AT (Completed) CZ (Prematurely Ended) DE (Completed) SK (Completed) HU (Completed) FI (Completed) PT (Completed) GR (Completed) PL (Completed) IE (Completed) IT (Completed) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011817-26 | Sponsor Protocol Number: BHS-UCB2009 | Start Date*: 2010-10-21 |
Sponsor Name:UZ Brussel VUB | ||
Full Title: A pilot study to assess the feasibility of unrelated umbilical cord blood transplantation with coinfusion of third-party mesenchymal stem cells after myeloablative or nonmyeloablative conditioning ... | ||
Medical condition: Adult patients with hematological malignancies | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004896-60 | Sponsor Protocol Number: LUMC2015-02 | Start Date*: 2015-11-26 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Decitabine-cytarabine chemotherapy in elderly AML and high risk MDS patients (> 65 years) with high early mortality risk | ||
Medical condition: Acute myeloid leukemia and high risk myelodysplasia | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002460-13 | Sponsor Protocol Number: VITDALIZE | Start Date*: 2017-01-03 |
Sponsor Name:Medical University of Graz | ||
Full Title: Effect of high-dose vitamin D3 on 28-day mortality in adult critically ill patients with severe vitamin D deficiency: a multicenter, placebo-controlled double-blind phase III RCT | ||
Medical condition: Adult critically ill patients with severe vitamin D deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002671-34 | Sponsor Protocol Number: PI20208430057 | Start Date*: 2020-12-04 |
Sponsor Name:CHU Amiens-Picardie | ||
Full Title: Comparison of Landiolol versus standard of care for prevention of mortality in patients hospitalized for a septic shock with hypercontractlity: an open label prospective randomized study | ||
Medical condition: septic shock with hypercontractlity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
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: 2021-002505-10 | Sponsor Protocol Number: NL77754.018.21 | Start Date*: 2021-11-30 | |||||||||||||||||||||
Sponsor Name:Amsterdam University Medical Centre | |||||||||||||||||||||||
Full Title: Rescue Alkaline Phosphatase In Defense against all cause Acute Kidney Injury (RAPID-AKI) | |||||||||||||||||||||||
Medical condition: Acute kidney injury | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
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