Related trials
		 
			
				 
				
					BASKET-PROVE (SES), 2010 - sirolimus eluting stent  vs bare-metal stent
				
			 
			
				 
				
					GISSOC II, 2010 - sirolimus eluting stent  vs bare-metal stent
				
			 
			
				 
				
					RESOLUTE All comers, 2010 - zotarolimus eluting stent  vs everolimus eluting stent
				
			 
			
				 
				
					SORT-OUT-3, 2010 - zotarolimus eluting stent  vs sirolimus eluting stent
				
			 
			
				 
				
					SPIRIT IV, 2010 - everolimus eluting stent  vs paclitaxel eluting stent
				
			 
			
				 
				
					BASKET-PROVE (EES), 2010 - everolimus eluting stent  vs bare-metal stent
				
			 
			
				 
				
					ISAR TEST 2 (vs ZES), 2009 - dual sirolimus, probucol eluting stent  vs zotarolimus eluting stent
				
			 
			
				 
				
					Thiele, 2009 - sirolimus ES  vs MIDCAB
				
			 
			
				 
				
					ENDEAVOR IV, 2009 - zotarolimus eluting stent  vs paclitaxel eluting stent
				
			 
			
				 
				
					ZEST AMI (vs PES), 2009 - zotarolimus eluting stent  vs paclitaxel eluting stent
				
			 
			
				 
				
					COMPARE, 2009 - everolimus eluting stent  vs paclitaxel eluting stent
				
			 
			
				 
				
					ISAR TEST 2 (vs SES), 2009 - dual sirolimus, probucol eluting stent  vs sirolimus eluting stent
				
			 
			
				 
				
					ZEST (vs PES), 2009 - zotarolimus eluting stent  vs paclitaxel eluting stent
				
			 
			
				 
				
					ZEST (vs SES), 2009 - zotarolimus eluting stent  vs sirolimus eluting stent
				
			 
			
				 
				
					ISAR TEST 3 (BP), 2009 - sirolimus biodegradable polymer  vs sirolimus eluting stent
				
			 
			
				 
				
					ISAR-TEST-4 (biodegradable polymer), 2009 - sirolimus biodegradable polymer  vs sirolimus eluting stent
				
			 
			
				 
				
					GENIUS-STEMI, 2009 - Genous stent  vs bare-metal stent
				
			 
			
				 
				
					SYNTAX, 2009 - paclitaxel eluting stent  vs CABG
				
			 
			
				 
				
					PASEO, 2009 - drug-eluting stents  vs bare-metal stent
				
			 
			
				 
				
					ISAR TEST 3 (PF), 2009 - polymer free sirolimus stent  vs sirolimus eluting stent
				
			 
			
				 
				
					DEBATER (SES vs BMS), 2009 - sirolimus eluting stent  vs bare-metal stent
				
			 
			
				 
				
					ISAR-LEFT-MAIN, 2009 - sirolimus eluting stent  vs paclitaxel eluting stent
				
			 
			
				 
				
					ZEST AMI (vs SES), 2009 - zotarolimus eluting stent  vs sirolimus eluting stent
				
			 
			
				 
				
					SORT OUT II, 2008 - sirolimus eluting stent  vs paclitaxel eluting stent
				
			 
			
				 
				
					DES-DIABETES, 2008 - sirolimus eluting stent  vs paclitaxel eluting stent
				
			 
		 
		 
		 
		
		See also:
		 
			
				
					All coronary artery disease clinical trials
				
			
		
			
			All clinical trials of Drug eluting stent 
			
		
		
			
			All clinical trials of zotarolimus eluting stent 
			
		
	 | 
	
		 
	 | 
	
	Treatments
	
	
		| Studied treatment | 
		
		Zotarolimus-eluting stents
		 
		
		Endeavor 
		
		 | 
	 
	
		| Control treatment | 
		
		sirolimus-eluting stents (SES)
		 
		
		Cypher
		
		 | 
	 
		
			| Concomittant treatment | 
			dual antiplatelet therapy for 12 months | 
		 
	 
	
	
	
	Patients
	
		
			| Patients | 
			Patients With Coronary Artery Disease undergoing PCI for any indication | 
		 
		
			| Exclusion criteria | 
			inability to provide informed consent; life expectancy 
		 |  
				| Baseline characteristics | 
					
					
						
							| age | 
							64.3%  | 
						 
						
							| history of MI  (%) | 
							26.5%  | 
						 
						
							| diabetes (%) | 
							14%  | 
						 
						
							| unstable angina  (%) | 
							38%  | 
						 
						
							| lesion length (mm) | 
							13.5 mm  | 
						 
						
							| male (%) | 
							72.5%  | 
						 
						
							| Female (%) | 
							26%  | 
						 
						
							| STEMI | 
							7%  | 
						 
						
							| Stable angina | 
							52%  | 
						 
						
							| No of lesions per patients | 
							1.55  | 
						 
					 						
					 | 
				 
	 
	
	
	
	
	
	
	Method and design
	
	
		| Randomized effectives | 
		1162 / 1171 (studied vs. control) | 
	 
		
			| Design | 
			Parallel groups | 
		 
		
			| Blinding | 
			open | 
		 
		
			| Follow-up duration | 
			9 months (18 mo) | 
		 
		
			| Hypothesis | 
			Superiority | 
		 
		
			| Primary endpoint | 
			MACE | 
		 
	
	 
	
	
	
	
	
	
	
  
	Results	
	
	
	
		
	
	
		
			Endpoint
		
	
	
		
		Studied treat. n/N
			
	
	
		
		Control treat. n/N
		
	
	
		
			Graph
		
	
	
		
			RR [95% CI]
		
	
	
		
			
				
				All cause death
				 
			
		
			
				
				NA / 1162 
				
			
			
				
				NA / 1171 
				
			
		
			
				
					
						classic
					
					
					
				
			
				
				
			
			
		
			
				
					1,45 [0,76;2,77]
				
			
	
	
		
			
				
				cardiac death
				 
			
		
			
				
				NA / 1162 
				
			
			
				
				NA / 1171 
				
			
		
			
				
					
						classic
					
					
					
				
			
				
				
			
			
		
			
				
					1,51 [0,73;3,13]
				
			
	
	
		
			
				
				MI (fatal and non fatal)
				 
			
		
			
				
				NA / 1162 
				
			
			
				
				NA / 1171 
				
			
		
			
				
					
						classic
					
					
					
				
			
			
			
		
			
				
					3,47 [1,15;10,48]
				
			
	
	
		
			
				
				target lesion revascularisation 
				 
			
		
			
				
				NA / 1162 
				
			
			
				
				NA / 1171 
				
			
		
			
				
					
						classic
					
					
					
				
			
			
			
		
			
				
					4,19 [2,12;8,28]
				
			
	
	
		
			
				
				Stent thrombosis (any, end of follow up)
				 
			
		
			
				
				NA / 1162 
				
			
			
				
				NA / 1171 
				
			
		
			
				
					
						classic
					
					
					
				
			
			
			
		
			
				
					4,62 [1,34;15,93]
				
			
	
	
		
			
				
				2 yr Death (all cause) 
				 
			
		
			
				
				NA / 1162 
				
			
			
				
				NA / 1171 
				
			
		
			
				
					
						classic
					
					
					
				
			
				
				
			
			
		
			
				
					1,61 [1,03;2,51]
				
			
	
	
		
			
				
				2 yr MACE 
				 
			
		
			
				
				NA / 1162 
				
			
			
				
				NA / 1171 
				
			
		
			
				
					
						classic
					
					
					
				
			
			
			
		
			
				
					2,19 [1,58;3,04]
				
			
	
	
		
			
				
				2 yr TLR 
				 
			
		
			
				
				NA / 1162 
				
			
			
				
				NA / 1171 
				
			
		
			
				
					
						classic
					
					
					
				
			
			
			
		
			
				
					3,66 [2,23;6,01]
				
			
	
	
		
		
		
		
		
			
				0
			
		
		
		
		
		
				2
		
		
		
		
		
			1.0
		
	
  
 
	 
		
	
		
		
				
					| 
						Relative risks
					 | 
				 
			
			| Endpoint | 
			Events (%) | 
			Relative Risk | 
			95% CI | 
			Endpoint definition in the trial | 
			Ref | 
			 
			
			| Studied treat. | 
			Control treat. | 
			 
					
					
					
					
					
					
					
					
					
					
					
					
					
					
					
					
					
					
					
					
					
					
		
			| 
			The primary endpoint (if exists) appears in blod characters
			 | 
		 
		
			| 
			Reference(s) used for data extraction: 
				
					0: 
				
			 | 
		 
		 
		
		
			
			| Endpoint | 
			studied treat. | 
			control treat. | 
			mean diff | 
			 
		 
	 
	
	
	
				
					| 
						Absolute risk reduction 
					 | 
				 
	
		| Endpoint | 
		Events rate | 
		Absolute risk reduction (ARR) | 
	 
	
		| Studied treat. | 
		Control treat. | 
	 
	 	
	 
Meta-analysis of all similar trials: 
			
				
					Drug eluting stent in coronary artery disease for acute myocardial infarction
				
			 
			
				
					Drug eluting stent in coronary artery disease for all type of patients
				
			 
	
  
	
	
	
	
	
	
	
	
	
	
	
		 
		Reference(s)
	
	
	
			- 
				
			    Rasmussen K, Maeng M, Kaltoft A, Thayssen P, Kelbæk H, Tilsted HH, Abildgaard U, Christiansen EH, Engstrøm T, Krusell LR, Ravkilde J, Hansen PR, Hansen KN, Abildstrøm SZ, Aarøe J, Jensen JS, Kristensen SD, Bøtker HE, Madsen M, Johnsen SP, Jensen LO, Søren. 
			    Efficacy and safety of zotarolimus-eluting and sirolimus-eluting coronary stents in routine clinical care (SORT OUT III): a randomised controlled superiority trial..
			    Lancet 2010 Mar 13;:
					- 10.1016/S0140-6736(10)60208-5
			    
 
				
					 
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