Mesalazine modified-release tablets in the treatment of ulcerative colitis in remission phase: a multi-center, single-blinded and randomized controlled study
	    		
		   		
		   			 
		   		
	    	
    	 
    	10.3760/cma.j.issn.0254-1432.2015.04.009
   		
        
        	
        		- VernacularTitle:美沙拉秦缓释片治疗缓解期溃疡性结肠炎的多中心、单盲、随机对照研究
- Author:
	        		
		        		
		        		
			        		Jing SUN
			        		
			        		;
		        		
		        		
		        		
			        		Yaozong YUAN
			        		
			        		
		        		
		        		
		        		
 
			        		
			        		
		        		 
- Publication Type:Journal Article
- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Mesalazine;
			        		
			        		
			        		
				        		Colitis,ulcerative;
			        		
			        		
			        		
				        		Randomized controlled trial
			        		
			        		
	        			
        			
        		
- From:
	            		
	            			Chinese Journal of Digestion
	            		
	            		 2015;35(4):256-259
	            	
            	
- CountryChina
- Language:Chinese
- 
		        	Abstract:
			       	
			       		
				        
				        	Objective To evaluate the efficacy and safety of mesalazine modified-release tablets in the maintenance treatment of patients with ulcerative colitis (UC) in remission phase.Methods This study was a multi-center,single-blinded and randomized controlled study.From November 2010 to August 2012,251 patients with UC from 18 hospitals were enrolled.According to the randomization table,all patients were divided into the mesalazine modified-release tablets group (n 126) and the mesalazine enteric-coated tablets group (n=125).The course of treatment were both 48 weeks.The primary efficacy parameter of the two groups including the rate of non-recurrence of bloody stool,and the secondary efficacy parameter including period of non-recurrence of bloody stool,period of non-recurrence of UC,incidence of adverse events and adverse drug reactions were observed.The GENMOD model was applied to calculate 95% confidence interval (CI) of the rate of non-recurrence of bloody stool of the two groups.If the lower limits was over-10% of the setting,it indicated that the former was not inferior to the latter.Results In 48 weeks of maintenance treatment,the rate of non-recurrence of bloody stool of themesalazinemodified-release tablets group was 82.99%(95%CI 73.53% to 92.45%) and 73.30% (95% CI 64.04% to 82.56%) in the mesalazine enteric-coated tablets group,respectively,and the difference between the two groups was 9.69%(95%CI-1.15% to 20.53% (>-10%)) which indicated the mesalazine modified-release tablets group was not inferior to the mesalazine enteric-coated tablets group.There was no significant difference in the period of non recurrence of bloody stool and period of non recurrence of UC between the two groups (both P>0.05).The incidence of adverse events was 48.78% (60/123) in the mesalazine modified-release tablets group and 48.00% (60/125) in the mesalazine enteric-coated tablets group,and the difference was not statistically significant (P=0.902).The incidence of adverse reactions was 16.26 % (20/123) in the mesalazine modified release tablets group and 13.60 % (17/125) in the mesalazine enteric-coated tablets group.There was no statistically significant difference (P =0.556).Conclusion Mesalazine modified release tablets can help maintain long-term remission in patients with UC,and can be used as a safe and effective alternative medicine in the treatments of UC in remission phase.