| 
 
		
		Related trials
		 
				 ENGAGE-AF TIMI 48 High dose, 2013 - edoxaban  vs warfarin standard dose 
				 AVERROES, 2011 - apixaban  vs aspirin 
				 ARISTOTLE, 2011 - apixaban  vs warfarin standard dose 
				 ROCKET-AF, 2010 - rivaroxaban  vs warfarin standard dose 
				 ACTIVE A, 2009 - aspirin + clopidogrel  vs aspirin 
				 RE-LY (150mg), 2009 - dabigatran 150mg  vs warfarin standard dose 
				 RE-LY (110mg), 2009 - dabigatran 110mg  vs warfarin standard dose 
				 Lip (phase 2 AZD0837), 2009 - AZD0837  vs warfarin standard dose 
				 AMADEUS, 2008 - idraparinux  vs warfarin standard dose 
				 PETRO (150mg), 2007 - dabigatran 150mg  vs warfarin standard dose 
				 Japanese AF Trial, 2006 - aspirin  vs control 
				 ACTIVE W, 2006 - aspirin + clopidogrel  vs anticoagulant 
				 SPORTIF  V, 2005 - ximelagatran  vs warfarin standard dose 
				 NASPEAF (triflusal vs coumadin standard dose)), 2004 - triflusal  vs coumadin standard dose 
				 NASPEAF (triflusal + coumadin medium dose vs coumadin standard dose), 2004 - triflusal+coumadin medium dose  vs coumadin standard dose 
				 NASPEAF (triflusal+coumadin medium dose vs triflusal), 2004 - triflusal+coumadin medium dose  vs triflusal 
				 SAFT(warfarin low dose + aspirin vs no treatment), 2003 - warfarin low dose + aspirin  vs control 
				 SPORTIF III, 2003 - ximelagatran  vs warfarin standard dose 
				 SPORTIF II (ximelagatran vs warfarin standard dose), 2002 - ximelagatran  vs warfarin standard dose 
				 PATAF (coumadin low dose vs coumadin standard dose), 1999 - coumadin low dose  vs coumadin standard dose 
				 PATAF (vs coumadin standard dose), 1999 - aspirin  vs coumadin standard dose 
				 LASAF(aspirin vs no treatment), 1999 - aspirin  vs control 
				 PATAF  (vs coumadin low dose), 1999 - aspirin  vs coumadin low dose 
				 AFASAK II (aspirin vs warfarin low dose), 1998 - aspirin  vs warfarin low dose 
				 AFASAK II (warfarin low dose+aspirin vs warfarin standard dose), 1998 - warfarin + aspirin  vs warfarin standard dose 
 
 
		See also:
		All atrial fibrillation clinical trials
				
			
		
			
			All clinical trials of new oral anticoagulants 
			
		
		
			
			All clinical trials of apixaban |  | 
	Treatments
	
		| Studied treatment | apixaban 5mg twice daily 
 |  
		| Control treatment | warfarin adjusted for an INR between 2 and 3 
 |  | Treatments description | 
						
						| time within the therapeutic range (%) | mean 62% (median 66%) |  |  Patients
		
			| Patients | subjects with atrial fibrillation and risk factors for stroke |  
			| Inclusion criteria | males and females >= 18 yrs with AF and one or more of the following risk factors for stroke:  age ¡Ý 75, previous stroke  TIA or Systemic Embolism  Symptomatic congestive heart failure or left ventricular dysfunction with LVEF |  | Baseline characteristics | 
						
							| age(mean) | 70 yrs (median) |  
							| male(%) | 65% |  
							| weight(mean) | 82 kg (median) |  
							| systolic blood pressure(mean) | 130 mmHg (median) |  
							| hypertension(%) | 87.5% |  
							| diabete mellitus(%) | 25% |  
							| prior TIA or stroke(%) | 19.45% |  
							| left ventricular dysfunction(%) | 35.5% |  
							| prior myocardial infarction(%) | 14.2% |  
							| paroxysmal AF(%) | 15.3% |  
							| subgroup test | a |  
							| CHADS2 Score (mean) | 2.1 |  
							| CHADS2 Score = 2 (%) | 35.8% |  
							| CHADS2 Score = 3 (%) | 30.2% |  |  Method and design
	
		| Randomized effectives | 9120 / 9081 (studied vs. control) |  
			| Design | Parallel groups |  
			| Blinding | double blind |  
			| Follow-up duration | 1.8 yrs (median) |  
			| Number of centre | 1034 |  
			| Geographic area | 39 countries |  
			| Hypothesis | Non inferiority |  
			| Primary endpoint | stroke or systemic embolism |  
			| Remarks |  |  Remarks / Comments
 Results
	
		
	
	
		
			Endpoint
		
	
	
		
		Studied treat.n/N
			
	
	
		
		Control treat.
 n/N
		
	
	
		
			Graph
		
	
	
		
			RR [95% CI]
 
				Coronary event
				90 / 9088 102 / 9052
 0,88 [0,66;1,17]
 
				thrombo-embolic event (cerebral or systemic)
				212 / 9120 265 / 9081
 0,80 [0,67;0,95]
 
				systemic thrombo-embolic complication 
				15 / 9120 17 / 9081
 0,88 [0,44;1,76]
 
				stroke (fatal and non fatal) 
				199 / 9120 250 / 9081
 0,79 [0,66;0,95]
 
				ischemic stroke 
				162 / 9120 175 / 9081
 0,92 [0,75;1,14]
 
				myocardial  infarction (fatal and non fatal) 
				90 / 9120 102 / 9081
 0,88 [0,66;1,16]
 
				All cause death
				603 / 9120 669 / 9081
 0,90 [0,81;1,00]
 
				Bleeding
				2356 / 9120 3060 / 9081
 0,77 [0,73;0,80]
 
				Major bleeding
				327 / 9120 462 / 9081
 0,70 [0,61;0,81]
 
				Haemmorhagic stroke
				40 / 9120 78 / 9081
 0,51 [0,35;0,75]
 
				Gastrointestinal major bleeding 
				105 / 9120 119 / 9081
 0,88 [0,68;1,14]
 
				major or clinically relevant non-major bleeding
				613 / 9120 877 / 9081
 0,70 [0,63;0,77]
 
				intracranial hemorrhage
				52 / 9120 122 / 9081
 0,42 [0,31;0,59]
				
			
	
	
		
		
		
		
		
			
				0
			
		
		
		
		
		
				2
		
		
		
		
		
			1.0
 
		
		
				
					| Relative risks |  
			| Endpoint | Events (%) | Relative Risk | 95% CI | Endpoint definition in the trial
 | Ref |  
			| Studied treat. | Control treat. |  
						| Coronary event | 90 / 9088 (1,0%) | 102 / 9052 (1,1%) | 0,88 | [0,66;1,17] |  | 16949 |  
						| thrombo-embolic event (cerebral or systemic) | 212 / 9120 (2,3%) | 265 / 9081 (2,9%) | 0,80 | [0,67;0,95] | ITT population | 14873 |  
						| systemic thrombo-embolic complication | 15 / 9120 (0,2%) | 17 / 9081 (0,2%) | 0,88 | [0,44;1,76] |  | 14873 |  
						| stroke (fatal and non fatal) | 199 / 9120 (2,2%) | 250 / 9081 (2,8%) | 0,79 | [0,66;0,95] |  | 14873 |  
						| ischemic stroke | 162 / 9120 (1,8%) | 175 / 9081 (1,9%) | 0,92 | [0,75;1,14] | Ischemic or uncertain type of stroke | 14873 |  
						| myocardial  infarction (fatal and non fatal) | 90 / 9120 (1,0%) | 102 / 9081 (1,1%) | 0,88 | [0,66;1,16] |  | 14873 |  
						| All cause death | 603 / 9120 (6,6%) | 669 / 9081 (7,4%) | 0,90 | [0,81;1,00] |  | 14873 |  
						| Bleeding | 2356 / 9120 (25,8%) | 3060 / 9081 (33,7%) | 0,77 | [0,73;0,80] |  | 14873 |  
						| Major bleeding | 327 / 9120 (3,6%) | 462 / 9081 (5,1%) | 0,70 | [0,61;0,81] | ISTH major bleeding | 14873 |  
						| Haemmorhagic stroke | 40 / 9120 (0,4%) | 78 / 9081 (0,9%) | 0,51 | [0,35;0,75] | Hemorrhagic stroke | 14873 |  
						| Gastrointestinal major bleeding | 105 / 9120 (1,2%) | 119 / 9081 (1,3%) | 0,88 | [0,68;1,14] |  | 14873 |  
						| major or clinically relevant non-major bleeding | 613 / 9120 (6,7%) | 877 / 9081 (9,7%) | 0,70 | [0,63;0,77] |  | 14873 |  
						| intracranial hemorrhage | 52 / 9120 (0,6%) | 122 / 9081 (1,3%) | 0,42 | [0,31;0,59] | ISTH major bleeding | 14873 |  
			| The primary endpoint (if exists) appears in blod characters |  
			| Reference(s) used for data extraction: 
				
					14873: Granger CB, Alexander JH, McMurray JJ, Lopes RD, Hylek EM, Hanna M, Al-Khalidi HR, Ansell J, Atar D, Avezum A, Bahit MC, Diaz R, Easton JD, Ezekowitz JA, Flaker G, Garcia D, Geraldes M, Gersh BJ, Golitsyn S, Goto S, Hermosillo AG, Hohnloser SH, Horowitz JApixaban versus Warfarin in Patients with Atrial Fibrillation.N Engl J Med 2011 Aug 27;:
				
				
					16949: Mak KHCoronary and mortality risk of novel oral antithrombotic agents: a meta-analysis of large randomised trials.BMJ Open 2012;2: |  
			
			| Endpoint | studied treat. | control treat. | mean diff |  
	
	
				
					| Absolute risk reduction (for a follow-up of 1.8 yrs (median)) |  
		| Endpoint | Events rate | Absolute risk reduction (ARR)
 |  
		| Studied treat. | Control treat. |  
				| Coronary event | 9,90‰ | 1,13% | -0,14% |  
				| thrombo-embolic event (cerebral or systemic) | 2,32% | 2,92% | -0,59% |  
				| systemic thrombo-embolic complication | 1,64‰ | 1,87‰ | -0,02% |  
				| stroke (fatal and non fatal) | 2,18% | 2,75% | -0,57% |  
				| ischemic stroke | 1,78% | 1,93% | -0,15% |  
				| myocardial  infarction (fatal and non fatal) | 9,87‰ | 1,12% | -0,14% |  
				| All cause death | 6,61% | 7,37% | -0,76% |  
				| Bleeding | 25,83% | 33,70% | -7,86% |  
				| Major bleeding | 3,59% | 5,09% | -1,50% |  
				| Haemmorhagic stroke | 4,39‰ | 8,59‰ | -0,42% |  
				| Gastrointestinal major bleeding | 1,15% | 1,31% | -0,16% |  
				| major or clinically relevant non-major bleeding | 6,72% | 9,66% | -2,94% |  
				| intracranial hemorrhage | 5,70‰ | 1,34% | -0,77% |  Meta-analysis of all similar trials: 
				
					antithrombotics in atrial fibrillation for primary prevention of thromboembolic events
				
			 
				
					direct factor Xa inhibitors in atrial fibrillation for all type of patients 
				
			 
				
					new oral anticoagulants in atrial fibrillation for all type of patients
				
			 
		 Reference(s)
	
		| TrialResults-center ID | TRC10339 |  
		| Trials register # | NCT00412984 |  
			
				
			    Lopes RD, Alexander JH, Al-Khatib SM, Ansell J, Diaz R, Easton JD, Gersh BJ, Granger CB, Hanna M, Horowitz J, Hylek EM, McMurray JJ, Verheugt FW, Wallentin L. 
			    Apixaban for reduction in stroke and other ThromboemboLic events in atrial fibrillation (ARISTOTLE) trial: design and rationale..
			    Am Heart J 2010;159:331-9
					- 10.1016/j.ahj.2009.07.035
			    
  Pubmed
				 
				|
				
					Hubmed
				
				| Fulltext
				
			    Granger CB, Alexander JH, McMurray JJ, Lopes RD, Hylek EM, Hanna M, Al-Khalidi HR, Ansell J, Atar D, Avezum A, Bahit MC, Diaz R, Easton JD, Ezekowitz JA, Flaker G, Garcia D, Geraldes M, Gersh BJ, Golitsyn S, Goto S, Hermosillo AG, Hohnloser SH, Horowitz J. 
			    Apixaban versus Warfarin in Patients with Atrial Fibrillation..
			    N Engl J Med 2011 Aug 27;:
					- 10.1056/NEJMoa1107039
			    
  Pubmed
				 
				|
				
					Hubmed
				
				| Fulltext 
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