- Trials with a EudraCT protocol (39)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    39 result(s) found for: Acenocoumarol.
                    
                
			
   			
		
		Displaying page 1 of 2.
	
	
	| EudraCT Number: 2016-003086-25 | Sponsor Protocol Number: 201600620 | Start Date*: 2017-04-19 | 
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: More precise dosing of acenocoumarol in patients aged 80 and above, a pilot study | ||
| Medical condition: atrial fibrillation venous thrombo-embolism heart valve repair other diseases with an indication for anticoagulation with vitamin K antagonists | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002291-41 | Sponsor Protocol Number: 1 | Start Date*: 2018-08-30 | 
| Sponsor Name:Gelderse Vallei Hospital | ||
| Full Title: The effect of administering VITamin K preprocedural on the vitamin K dependent coagulation factors and the INR in patients anticoagulated with ACEnocoumarol | ||
| Medical condition: Adult patients using acenocoumarol and planned to undergo an invasive procedure for which the effect of the anticoagulants should be reversed. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-004265-32 | Sponsor Protocol Number: 0206 | Start Date*: 2012-01-24 | |||||||||||
| Sponsor Name:Academic Medical Center | |||||||||||||
| Full Title: Left Ventricular Thrombus Formation after Acute Myocardial Infarction - a randomized multi-center trial comparing 2 different anti-thrombotic regimens | |||||||||||||
| Medical condition: Left Ventricular thrombus formation after acute myocardial infarction | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-002118-37 | Sponsor Protocol Number: HTAJ-TRANEX-2019-01 | Start Date*: 2021-06-17 | 
| Sponsor Name:Rafael Blancas-Gómez Casero | ||
| Full Title: MULTICENTER, DOUBLE BLIND CLINICAL TRIAL TO EVALUATE THE ANTIHEMORRAGIC EFFECT OF THE TOPICAL TRANEXAMIC ACID DURING PACEMAKER IN ANTICOAGULATED PATIENTS | ||
| Medical condition: Pacemaker implant for anticoagulated patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004494-96 | Sponsor Protocol Number: BAY 59-7939/IMP 11899 | Start Date*: 2007-03-19 | 
| Sponsor Name:Bayer HealthCare AG | ||
| Full Title: Once-daily oral direct factor Xa inhibitor rivaroxaban in the long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis or pulmonary emb... | ||
| Medical condition: Long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis or pulmonary embolism. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) ES (Completed) SE (Completed) DE (Completed) FI (Completed) FR (Completed) HU (Completed) AT (Completed) IT (Completed) DK (Completed) CZ (Completed) NL (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003398-16 | Sponsor Protocol Number: 6396 | Start Date*: 2017-02-15 | 
| Sponsor Name:Les Hôpitaux Universitaires de Strasbourg | ||
| Full Title: Study of the benefit / risk ratio of oral anticoagulation in hemodialysis patients with atrial fibrillation | ||
| Medical condition: - Renal failure with dialysis - atrial fibrillation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004495-13 | Sponsor Protocol Number: BAY 59-7939/11702 | Start Date*: 2007-03-12 | 
| Sponsor Name:Bayer Healthcare AG | ||
| Full Title: Oral direct factor Xa inhibitor rivaroxaban in patients with acute symptomatic deep-vein thrombosis or pulmonary embolism. | ||
| Medical condition: Treatment and secondary prevention of venous thromboembolism in patients with acute symptomatic deep- vein thrombosis or pulmonary embolism | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) ES (Completed) SE (Completed) FR (Completed) DE (Completed) FI (Completed) DK (Completed) HU (Completed) AT (Completed) IT (Completed) GB (Completed) CZ (Completed) NL (Completed) IE (Completed) LT (Completed) EE (Completed) LV (Completed) SK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-017256-27 | Sponsor Protocol Number: MUSICA-2 | Start Date*: 2010-04-05 | 
| Sponsor Name:Servicio de Cardiología. Hospital Universitario Vall d'Hebron | ||
| Full Title: Ensayo de eficacia y seguridad de la doble antiagregación comparada con la combinación de anticoagulación oral + doble antiagregación en pacientes con fibrilación auricular de bajo-moderado riesgo ... | ||
| Medical condition: Prevención de trombosis en pacientes con fibrilación auricular e implantación de stent coronario | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-006887-12 | Sponsor Protocol Number: HEPACO | Start Date*: 2011-12-07 | 
| Sponsor Name:Institut de Recerca HSCSP | ||
| Full Title: Randomized controlled trial to compare treatment with oral anticoagulation with vitamin K antagonists versus low molecular weight heparin (bemiparin) in patients with anticoagulation criteria and h... | ||
| Medical condition: Patients with gastrointestinal bleeding are not candidates for endoscopic treatment with oral anticoagulant previously. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004009-37 | Sponsor Protocol Number: MD2021.01 | Start Date*: 2021-11-05 | ||||||||||||||||
| Sponsor Name:Prothya Biosolutions BV | ||||||||||||||||||
| Full Title: A Phase 1/2 study of the dose-response in pharmacodynamics and safety of prothrombin complex concentrate Cofact in healthy subjects under vitamin K antagonist anticoagulation | ||||||||||||||||||
| Medical condition: Treatment of bleeding and perioperative prophylaxis | ||||||||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-003325-41 | Sponsor Protocol Number: 668353 | Start Date*: 2017-06-09 | 
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: PREemptive Pharmacogenomic testing for Preventing Adverse drug REactions | ||
| Medical condition: Adverse drug reactions | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004199-11 | Sponsor Protocol Number: NOSTRADAMUS | Start Date*: 2007-02-16 | |||||||||||
| Sponsor Name:Academic Medical Center | |||||||||||||
| Full Title: NOSTRADAMUS: Testing for thrombophilia in patients with a first episode of venous thromboembolism: a randomized controlled trial to assess effects on clinical outcomes, quality of life, and costs. | |||||||||||||
| Medical condition: A randomized controlled trial of testing and no testing for thrombophilia in patients with a first episode of venous thrombosis or pulmonary embolism (venous thromboembolism, VTE) will be performed... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-015858-38 | Sponsor Protocol Number: ACENO-K-01-2009 | Start Date*: 2011-05-26 | 
| Sponsor Name:Dr. Antonio Javier Trujillo Santos | ||
| Full Title: Comparación de la adición de bajas dosis de vitamina K al tratamiento con acenocumarol frente al tratamiento tradicional con acenocumarol sobre la estabilidad del efecto anticoagulante y sus compli... | ||
| Medical condition: Pacientes que precisen de anticoagulación oral con cumarinas durante al menos 3 meses, fundamentalmente son pacientes con arritmias cardíacas (sobre todo fibrilación auricular) y enfermedad tromboe... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-016643-18 | Sponsor Protocol Number: FC/HULP_002 | Start Date*: 2010-03-18 | 
| Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario de La Paz | ||
| Full Title: Ensayo clínico randomizado para evaluar la eficiencia y efectividad de la dosificación individualizada de acenocumarol mediante un algoritmo farmacogenético versus ajuste estándar en pacientes que... | ||
| Medical condition: enfermedad tromboembólica venosa (ETEV: trombosis venosa profunda y tromboembolismo pulmonar). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-000392-33 | Sponsor Protocol Number: 2014PROPER3 | Start Date*: 2015-06-30 | |||||||||||
| Sponsor Name:University Medical Center Groningen | |||||||||||||
| Full Title: Fixed versus variable dosing strategy of prothrombin complex concentrate for bleeding complications of vitamin K antagonists | |||||||||||||
| Medical condition: Major bleeding complications of vitamin K antagonists | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004805-14 | Sponsor Protocol Number: 2013-0001 | Start Date*: 2014-08-14 | 
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: Vitamin K antagonist (VKA)versus New Oral Anticoagulants (NOACs) in patients with currently well controlled VKA therapy for non-valvular atrial fibrillation: a pilot study | ||
| Medical condition: non-valvular atrial fibrillation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-000393-11 | Sponsor Protocol Number: NL60426 | Start Date*: 2017-09-07 | 
| Sponsor Name:University Medical Center utrecht | ||
| Full Title: ’Switching anticoagulant management from a VKA to a NOAC-based treatment strategy in frail elderly patients with atrial fibrillation (FRAIL-AF study) | ||
| Medical condition: Atrial Fibrilation | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-002586-12 | Sponsor Protocol Number: 1160.63 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: Twice-daily oral direct thrombin inhibitor dabigatran in the long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis or pulmonary embo... | |||||||||||||
| Medical condition: long-term prevention of recurrent symptomatic venous thromboembolism (VTE) in patients with symptomatic deep-vein thrombosis (DVT) or pulmonary embolism (PE) who completed 6 to 18 months of treatme... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) AT (Completed) IT (Completed) PL (Completed) CZ (Completed) NL (Completed) BE (Completed) LT (Completed) LV (Completed) EE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016992-31 | Sponsor Protocol Number: COU-001A | Start Date*: 2010-03-19 | |||||||||||||||||||||
| Sponsor Name:Democritus Universityof Thrace Medical School [...] | |||||||||||||||||||||||
| Full Title: EUropean Pharmacogenetics of AntiCoagulation Therapy trial | |||||||||||||||||||||||
| Medical condition: Newly diagnosed patients with venous tromboembolism (VTE) or atrial fibrillation (AF) requiring oral anticoagulation with phenprocoumon. | |||||||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2014-002442-45 | Sponsor Protocol Number: AXAFA-AFNET5 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
| Sponsor Name:Kompetenznetz Vorhofflimmern e.V. [Atrial Fibrillation NETwork (AFNET)] | ||||||||||||||||||||||||||||
| Full Title: Anticoagulation using the direct factor Xa inhibitor apixaban during Atrial Fibrillation catheter Ablation: Comparison to vitamin K antagonist therapy. | ||||||||||||||||||||||||||||
| Medical condition: Atrial fibrillation catheter ablation | ||||||||||||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) BE (Completed) DK (Completed) GB (Completed) NL (Completed) ES (Completed) AT (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
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