- Trials with a EudraCT protocol (57)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
57 result(s) found for: Levosimendan.
Displaying page 1 of 3.
| EudraCT Number: 2012-004979-39 | Sponsor Protocol Number: 8.1 | Start Date*: 2014-12-19 |
| Sponsor Name:VieCuri Medical Center | ||
| Full Title: Levosimendan in Acute Kidney Injury Study, a prospective, randomized, monocenter, double blind, placebo-controlled study to investigate the efficacy and safety of Levosimendan in Intensive Care Pat... | ||
| Medical condition: Acute Kidney Injury (AKI) in adult ICU patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001623-39 | Sponsor Protocol Number: Levo1010 | Start Date*: 2018-07-26 |
| Sponsor Name:Verein zur Förderung der Forschung auf dem Gebiet der Arteriosklerose, Thrombose und vaskulären Biologie (ATVB) | ||
| Full Title: Assessment of body composition changes after Levosimendan treatment in patients with advanced heart failure | ||
| Medical condition: Advanced heart failure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001702-30 | Sponsor Protocol Number: 200175 | Start Date*: 2022-02-08 |
| Sponsor Name:APHP | ||
| Full Title: « Use of Levosimendan as treatment of aneurysmal SubArachnoid Hemorrhage » | ||
| Medical condition: subarachnoid hemorrhages of aneurysmal origin (HSAa) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000588-26 | Sponsor Protocol Number: ICCE12.001 | Start Date*: 2012-10-16 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: Pharmacokinetics of Levosimendan in children with acute heart failure | ||
| Medical condition: Acute heart failure in children | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) FI (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-007407-86 | Sponsor Protocol Number: LevoRep | Start Date*: 2009-09-14 | |||||||||||
| Sponsor Name:Medizinische Universität Innsbruck - Universitätsklinik für Innere Medizin III | |||||||||||||
| Full Title: Efficacy and safety of pulsed infusions of levosimendan in outpatients with advanced heart failure | |||||||||||||
| Medical condition: Chronic heart failure | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) GR (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004063-31 | Sponsor Protocol Number: FIM-PRELEVD-2018-01 | Start Date*: 2019-04-26 |
| Sponsor Name:Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud (FIMABIS) | ||
| Full Title: Mechanisms of cardio and nephroprotection in patients who are going on cardiac surgery with right ventricular dysfunction, with preoperative treatment of levosimendan compared with placebo. (PREL... | ||
| Medical condition: Perioperative right ventricle dysfunction | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-007953-30 | Sponsor Protocol Number: cv-07/126 | Start Date*: 2008-02-11 |
| Sponsor Name:Fundación Investigación y Desarrollo en el Área Cardiovascular | ||
| Full Title: Levosimendan como agente inmunomodulador en la insuficiencia cardiaca aguda. Estudio Piloto Levosimendan as an immunomodulatory agent in acute heart failure. Pilot study. | ||
| Medical condition: Analysis of the short-term treatment with levosimendan, a cardiac stimulant drug, of the acute exacerbation of chronic heart failure Estudio del tratamiento a corto plazo con levosimendan, fármac... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-002431-80 | Sponsor Protocol Number: LEV1068 | Start Date*: 2006-09-15 | |||||||||||
| Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
| Full Title: Renal Effects of Levosimendan in Patients Admitted with Acute Decompensated Heart Failure | |||||||||||||
| Medical condition: Patients with acute decompensated heart failure. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004180-31 | Sponsor Protocol Number: 3119003 | Start Date*: 2019-04-29 | |||||||||||
| Sponsor Name:Orion Corporation | |||||||||||||
| Full Title: Effects of oral Levosimendan (ODM-109) on respiratory function in patients with ALS: open label extension for patients completing study 3119002 | |||||||||||||
| Medical condition: Amyotrophic Lateral Sclerosis (ALS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Prematurely Ended) DE (Prematurely Ended) FI (Prematurely Ended) AT (Prematurely Ended) NL (Prematurely Ended) IE (Prematurely Ended) GB (GB - no longer in EU/EEA) FR (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007197-31 | Sponsor Protocol Number: 3001088 | Start Date*: 2008-04-22 | |||||||||||
| Sponsor Name:Orion Corporation Orion Pharma | |||||||||||||
| Full Title: EFFECTS OF ORAL LEVOSIMENDAN ON AMBULATORY ELECTROCARDIOGRAPHIC VARIABLES AND CEREBROVASCULAR REACTIVITY IN PATIENTS WITH RECENT STROKE OR TIA. A RANDOMISED, DOUBLE BLIND, PLACEBO-CONTROLLED, DOSE ... | |||||||||||||
| Medical condition: Stroke or TIA | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) SE (Prematurely Ended) HU (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-001225-16 | Sponsor Protocol Number: 3001077 | Start Date*: 2004-10-28 |
| Sponsor Name:Orion Pharma | ||
| Full Title: Survival of patients with acute heart failure in need of intravenous inotropic support; a multicentre parallel- group, randomised, double- blind, double- dummy study of levosimendan versus dobutami... | ||
| Medical condition: Acutely decompensated heart failure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-003589-25 | Sponsor Protocol Number: Levo-AKI | Start Date*: 2014-11-11 |
| Sponsor Name:Sahlgrenska Universitetssjukhuset/Sahlgrenska | ||
| Full Title: The effect of levosimendan, on renal blood flow, function and oxygen uptake during acute renal failure after cardiac surgery | ||
| Medical condition: Acute kidney injury postoperatively in connection with heart surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-005310-19 | Sponsor Protocol Number: PI-0697-2012 | Start Date*: 2013-06-05 |
| Sponsor Name:FUNDACION PARA LA INVESTIGACIÓN BIOSANITARIA DE ANDALUCIA ORIENTAL_ FPA | ||
| Full Title: Double-blind randomized clinical trial to evaluate the efficacy and safety of levosimendan as preischemic myocardial conditioner in pediatric cardiac surgery | ||
| Medical condition: Children aged 1 month to 14 years in the health area of the province of Granada who will be undergoing heart surgery with a clinical high risk of developing acute heart failure after surgery, treat... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-003628-42 | Sponsor Protocol Number: NBK182/1/2022 | Start Date*: 2023-03-24 | |||||||||||
| Sponsor Name:Medical University of Gdańsk | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Multicenter Study of Levosimendan Therapy in low ejection fraction Takotsubo Syndrome (LevoTako Trial) | |||||||||||||
| Medical condition: Takotsubo syndrome (TTS), also known as apical ballooning syndrome, Takotsubo cardiomyopathy, broken heart syndrome, and stress-induced cardiomyopathy, is a rare condition and accounts for 1–3% of ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2004-004225-10 | Sponsor Protocol Number: 3001081 | Start Date*: 2005-03-07 | |||||||||||
| Sponsor Name:Orion Pharma | |||||||||||||
| Full Title: Effects of peroral levosimendan in the prevention of further hospitalisations in patients with chronic heart failure. A randomised, double-blind, placebo-controlled, multi-centre, parallel-group study | |||||||||||||
| Medical condition: Cardiac Failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) LT (Completed) LV (Completed) EE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001461-27 | Sponsor Protocol Number: FIM-BGC-2014-01 | Start Date*: 2015-01-19 | |||||||||||
| Sponsor Name:FIMABIS | |||||||||||||
| Full Title: Evaluation of the effect of organic preservation with the use of levosimendan after cardiac surgery in patients with low output syndrom compared with dobutamine. | |||||||||||||
| Medical condition: Low cardiac output syndrome | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003105-25 | Sponsor Protocol Number: MiLe-1 | Start Date*: 2014-08-27 |
| Sponsor Name:Sahlgrenska University Hospital / The Queen Silvia Children´s Hospital | ||
| Full Title: The prophylactic effect of levosimendan in reducing acute kidney injury postoperatively in pediatric patients undergoing corrective heart surgery | ||
| Medical condition: Acute kidney injury postoperatively in connection with surgery for congenital heart disease | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Completed) FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002643-10 | Sponsor Protocol Number: HCA-2011_1 | Start Date*: 2012-01-17 |
| Sponsor Name:Heart Center Co. Tampere University Hospital | ||
| Full Title: Intracoronary administration of levosimendan in cardiac surgery patients | ||
| Medical condition: Dysfunction after opening of aortic cross-clamp in patients undergoing aortic valve and coronary artery bypass (AVR+CABG) operation. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004384-29 | Sponsor Protocol Number: Levosepsis1 | Start Date*: 2005-05-23 |
| Sponsor Name:Dr GED DEMPSEY, University Hospital Aintree | ||
| Full Title: Double blind randomised controlled trial of Levosimendan versus Dopexamine in septic shock | ||
| Medical condition: Septic Shock | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
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