- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Atrioventricular block.
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EudraCT Number: 2017-002475-26 | Sponsor Protocol Number: GD2CAR01 | Start Date*: 2017-12-22 | |||||||||||
Sponsor Name:IRCCS Ospedale Pediatrico Bambino Gesù | |||||||||||||
Full Title: Phase I/II study of anti-GD2 Chimeric Antigen Receptor-Expressing T cells in pediatric patients affected by High Risk and/or relapsed/refractory Neuroblastoma | |||||||||||||
Medical condition: High Risk and/or relapsed/refractory Neuroblastoma | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003861-39 | Sponsor Protocol Number: GLUCOTAVI | Start Date*: 2023-03-07 |
Sponsor Name:JUAN MIGUEL RUIZ NODAR | ||
Full Title: Glucocorticoid treatment in patients undergoing TAVI to reduce the incidence of atrioventricular block and pacemaker implantation | ||
Medical condition: aortic stenosis | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003912-99 | Sponsor Protocol Number: CMP-MYTHiC | Start Date*: 2023-05-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA AO OSPEDALE NIGUARDA CA' GRANDA | |||||||||||||
Full Title: Single-blinded randomized investigator-driven controlled trial to assess the efficacy of colchicine to treat patients with cardiomyopathy with myocarditis (chronic inflammatory cardiomyopathy) CMP... | |||||||||||||
Medical condition: Cardiomyopathy with myocarditis (chronic inflammatory cardiomyopathy) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002708-38 | Sponsor Protocol Number: 131313 | Start Date*: 2020-10-26 |
Sponsor Name:Department of Medical Science Gothenburg University | ||
Full Title: Optimized pharmacological treatment for broken heart (takotsubo) syndrome | ||
Medical condition: The medical condition is acute heart failure (Takotsubo syndrome) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002541-11 | Sponsor Protocol Number: P170912J | Start Date*: 2019-06-06 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Prevention of post-operative Atrial Fibrillation by BOTulinum toxin injections into epicardial fat pads around pulmonary veins in patients undergoing cardiac surgery | |||||||||||||
Medical condition: Adult patients with indication for conventional cardiac surgery (CABG, aortic replacement, or ascending aorta surgery) will be eligible | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001781-14 | Sponsor Protocol Number: POX-MVA-005 | Start Date*: 2006-04-11 | |||||||||||
Sponsor Name:Bavarian Nordic A/S | |||||||||||||
Full Title: A partially randomized, partially double-blind, placebo-controlled Phase II non-inferiority study to evaluate immunogenicity and safety of one and two doses of MVA-BN (IMVAMUNE™) smallpox vaccine i... | |||||||||||||
Medical condition: Healthy subjects - prevention of smallpox infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006297-28 | Sponsor Protocol Number: POX-MVA-023 | Start Date*: 2008-07-30 | |||||||||||
Sponsor Name:Bavarian Nordic A/S | |||||||||||||
Full Title: An open-label Phase II study to evaluate immunogenicity and safety of a single IMVAMUNE® booster vaccination two years after the last IMVAMUNE® vaccination in former POX-MVA-005 vaccinees | |||||||||||||
Medical condition: Healthy subjects - prevention of smallpox infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003613-19 | Sponsor Protocol Number: APHP210303 | Start Date*: 2021-12-07 |
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
Full Title: AbataCept for the treatment of immune-cHeckpoint inhibitors induced mYocarditiS | ||
Medical condition: All adult patients with cancer (all cancer types) treated by immune checkpoint inhibitors (anti-PD1, anti-PDL1, anti-CTLA4 monotherapies or combination) and presenting drug-induced myocarditis. The... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004263-36 | Sponsor Protocol Number: RPL554-010-2015 | Start Date*: 2016-12-07 | |||||||||||
Sponsor Name:Verona Pharma plc | |||||||||||||
Full Title: A Phase IIa, randomised, double blind, placebo controlled, three way crossover study to assess the pharmacokinetics of RPL554 administered to adult patients with Cystic Fibrosis. | |||||||||||||
Medical condition: Cystic Fibrosis (CF) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000388-18 | Sponsor Protocol Number: DIAS-001-FFR | Start Date*: 2016-03-24 | |||||||||||
Sponsor Name:Diasolve Ltd | |||||||||||||
Full Title: A randomised crossover investigation to evaluate and compare the effectiveness, safety and feasibility of a novel dedicated Over-The-Wire FFR Infusion MicroCatheter (HYPEREM IC) for measuring fract... | |||||||||||||
Medical condition: This is a single‐blind, randomised, crossover investigation comparing the investigational device using intra‐coronary (IC) Adenosine infusion to the standard intravenous (IV) infusion method used f... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001732-25 | Sponsor Protocol Number: PBF-680CT-06 | Start Date*: 2021-08-13 | |||||||||||
Sponsor Name:Palobiofarma, S.L | |||||||||||||
Full Title: A phase IIa, randomized, double blind, placebo-controlled study to assess the effect of PBF-680 in patients with moderate to severe COPD on top of standard medication. | |||||||||||||
Medical condition: Patients with moderate to severe Chronic Obstructive Pulmonar Disease (COPD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001466-37 | Sponsor Protocol Number: A-STAMI | Start Date*: 2021-07-08 | ||||||||||||||||
Sponsor Name:Västra Götalandsregionen, Sahlgrenska University Hospital | ||||||||||||||||||
Full Title: Adenosine’s effect on STunning resolution in Acute Myocardial Infarction | ||||||||||||||||||
Medical condition: Acute Myocardial Infarction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001245-32 | Sponsor Protocol Number: PGX-III-AP-002 | Start Date*: 2011-10-19 | |||||||||||
Sponsor Name:Forest Laboratories, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind Trial of Apadenoson for the Detection of Myocardial Perfusion Defects Using Single-Photon Emission Computed Tomography (SPECT) Myocardial Perfusion Imaging (MPI) | |||||||||||||
Medical condition: Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022338-10 | Sponsor Protocol Number: H9H-MC-JBAK | Start Date*: 2011-05-03 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Phase 2 Study of LY2157299 in Patients with Hepatocellular Carcinoma | |||||||||||||
Medical condition: Carcinoma, hepatocellular | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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