- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Extracorporeal Life Support.
Displaying page 1 of 1.
EudraCT Number: 2019-004125-24 | Sponsor Protocol Number: NL6979 | Start Date*: 2020-07-02 |
Sponsor Name:UMCG | ||
Full Title: Reduced Anticoagulation Targets in Extracorporeal life support | ||
Medical condition: Heart or lungfailure treated with ECMO | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002259-20 | Sponsor Protocol Number: CASUAL_ECMO | Start Date*: 2023-08-17 |
Sponsor Name:Medical University of Vienna | ||
Full Title: A three-arm randomized controlled non-inferiority pilot study Comparing Anticoagulation Strategies using Unfractionated heparin, Argatroban and Low-molecular-weight heparin for Extracorporeal Memb... | ||
Medical condition: patients with indication for extracorporeal membrane oxygenation therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022780-35 | Sponsor Protocol Number: 10-005 | Start Date*: 2011-07-06 | |||||||||||
Sponsor Name:THERAKOS, Inc. | |||||||||||||
Full Title: A Randomized Controlled Study of Extracorporeal Photopheresis (ECP) Therapy with UVADEX™ for the Treatment of Patients with Moderate to Severe Chronic Graft-versus-Host Disease (cGvHD) | |||||||||||||
Medical condition: Chronic graft-versus-host disease (cGvHD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) AT (Completed) ES (Completed) IT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004684-12 | Sponsor Protocol Number: iNO_Protocol_V1.1_16.07.17 | Start Date*: 2019-05-16 |
Sponsor Name:Lady Cilento Children's Hospital | ||
Full Title: Nitric Oxide during Cardio Pulmonary Bypass during surgery for congenital heart defects: A Randomised Controlled Trial. | ||
Medical condition: Congenital heart disease ranks still within the top causes of infant mortality in industrialized countries. Despite considerable advances over the past decade, the exposure to cardiopulmonary bypas... | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001167-93 | Sponsor Protocol Number: Sobi.IMMUNO-101 | Start Date*: 2020-03-27 | |||||||||||
Sponsor Name:SWEDISH ORPHAN BIOVITRUM AB (PUBL) | |||||||||||||
Full Title: A phase 2/3, randomized, open-label, parallel group, 3-arm, multicenter study investigating the efficacy and safety of intravenous administrations of emapalumab, an anti-interferon gamma (anti-IFN¿... | |||||||||||||
Medical condition: SARS-CoV-2 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001563-74 | Sponsor Protocol Number: PHRCN2018/LEVOHEARTSHOCK-LEVY/YB | Start Date*: 2020-07-24 | |||||||||||
Sponsor Name:CHRU de Nancy | |||||||||||||
Full Title: Effect of early use of levosimendan versus placebo on top of a conventional strategy of inotrope use on a combined morbidity-mortality endpoint in patients with cardiogenic shock. LevoHeartShock St... | |||||||||||||
Medical condition: Cardiogenic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001811-94 | Sponsor Protocol Number: M18-868 | Start Date*: 2022-01-28 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 3 Open-Label, Randomized, Controlled, Global Study of Telisotuzumab Vedotin (ABBV-399) Versus Docetaxel in Subjects with Previously Treated c-Met Overexpressing, EGFR Wildtype, Locally Adva... | |||||||||||||
Medical condition: C-Met overexpressing EGFR wildtype, non-squamous non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Trial now transitioned) CZ (Trial now transitioned) SE (Trial now transitioned) HU (Ongoing) RO (Ongoing) AT (Trial now transitioned) IT (Ongoing) NL (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005659-19 | Sponsor Protocol Number: RG_14-287 | Start Date*: 2015-10-21 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: A phase II study of the use of azacitidine for the treatment of patients with chronic graft-versus-host-disease who have failed therapy with corticosteroids | |||||||||||||
Medical condition: Chronic Graft versus Host Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001113-32 | Sponsor Protocol Number: CNS7056-010 | Start Date*: 2013-08-02 | |||||||||||
Sponsor Name:PAION UK Limited | |||||||||||||
Full Title: A Randomized, Single-blind Phase II Study Evaluating the Efficacy, Safety and Pharmacokinetics of Remimazolam in General Anesthesia in Adult Patients Undergoing Cardiac Surgery, Including Follow-up... | |||||||||||||
Medical condition: Anaesthesia in adult patients undergoing cardiac surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003210-13 | Sponsor Protocol Number: LYT-100-2020-02 | Start Date*: 2020-10-27 | |||||||||||
Sponsor Name:PureTech LYT 100, Inc. | |||||||||||||
Full Title: A Phase 2 Randomized, Double-blind, Placebo-controlled Trial and Open Label Extension to Evaluate the Safety and Efficacy of Deupirfenidone (LYT- 100) in Post-acute COVID-19 Respiratory Disease | |||||||||||||
Medical condition: COVID-19 respiratory disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004529-14 | Sponsor Protocol Number: VTL-308 | Start Date*: 2016-02-08 |
Sponsor Name:Vital Therapies, Inc. | ||
Full Title: A RANDOMIZED, OPEN-LABEL, MULTICENTER, CONTROLLED, PIVOTAL STUDY TO ASSESS SAFETY AND EFFICACY OF ELAD® IN SUBJECTS WITH ALCOHOL-INDUCED LIVER DECOMPENSATION (AILD) | ||
Medical condition: Alcohol-Induced Liver Decompensation (AILD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) DE (Prematurely Ended) IE (Prematurely Ended) AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-015002-19 | Sponsor Protocol Number: VTI-206 | Start Date*: 2010-01-18 | |||||||||||
Sponsor Name:VITAL THERAPIES INCORPORATED | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ELAD IN SUBJECTS WITH ACUTE ON CHRONIC HEPATITIS (AOCH) | |||||||||||||
Medical condition: Acute on Chronic Hepatitis (AOCH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001884-21 | Sponsor Protocol Number: VTI-210 | Start Date*: 2013-07-26 | |||||||||||
Sponsor Name:VITAL THERAPIES INCORPORATED | |||||||||||||
Full Title: A RANDOMIZED, OPEN-LABEL, MULTICENTER, CONTROLLED STUDY TO ASSESS SAFETY AND EFFICACY OF ELAD IN SUBJECTS WITH SEVERE ACUTE ALCOHOLIC HEPATITIS (SAAH) AND LILLE SCORE FAILURE | |||||||||||||
Medical condition: Severe Acute Alcoholic Hepatitis (sAAH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003278-37 | Sponsor Protocol Number: INSIGHT-014-ACTIV-3 | Start Date*: 2020-09-04 | ||||||||||||||||
Sponsor Name:Regents of the University of Minesota | ||||||||||||||||||
Full Title: A Multicenter, Adaptive, Randomized, Blinded Controlled Trial of the Safety and Efficacy of Investigational Therapeutics for Hospitalized Patients with COVID-19 | ||||||||||||||||||
Medical condition: Subjects infected with SARS-CoV-2, admitted to the hospital due to COVID-19. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) GB (GB - no longer in EU/EEA) SE (Prematurely Ended) PL (Completed) GR (Ongoing) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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