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.