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Efficacy and Safety of Tiropramide in the Treatment of Patients With Irritable Bowel Syndrome: A Multicenter, Randomized, Double-blind, Non-inferiority Trial, Compared With Octylonium

Authors
Lee, Kang NyeongLee, Oh YoungChoi, Myung-GyuSohn, Chong IlHuh, Kyu ChanPark, Kyung SikKwon, Joong GooKim, NayoungRhee, Poong-LyulMyung, Seung-JaeLee, Joon SeongLee, Kwang JaePark, HyojinLee, Yong ChanChoi, Suck CheiJung, Hye-KyungJee, Sam RyongChoi, Chang HwanKim, Gwang HaPark, Moo InSung, In Kyung
Issue Date
Jan-2014
Publisher
대한소화기 기능성질환∙운동학회
Keywords
Irritable bowel syndrome; Antispasmodic; Octylonium; Rome III criteria; Tiropramide
Citation
Journal of Neurogastroenterology and Motility (JNM), v.20, no.1, pp 113 - 121
Pages
9
Indexed
SCIE
SCOPUS
KCI
Journal Title
Journal of Neurogastroenterology and Motility (JNM)
Volume
20
Number
1
Start Page
113
End Page
121
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/160886
DOI
10.5056/jnm.2014.20.1.113
ISSN
2093-0879
2093-0887
Abstract
Background/Aims Antispasmodics such as octylonium are widely used to manage irritable bowel syndrome (IBS) symptoms. However, the efficacy and safety of another antispasmodic, tiropramide, remain uncertain. We aimed to evaluate the efficacy and safety of tiropramide compared with octylonium in patients with IBS. Methods In this multicenter, randomized, non-inferiority trial, 287 patients with IBS (143 receiving tiropramide and 144 octylonium) were randomly allocated to either tiropramide 100 mg or octylonium 20 mg t.i.d (means 3 times a day) for 4 weeks. Primary endpoint was the mean change of abdominal pain from baseline assessed by visual analogue scales (VAS) score after 4 weeks of treatment. Secondary endpoints were the changes in abdominal pain from baseline at week 2 and in abdominal discomfort at weeks 2 and 4, using VAS scores, patient-reported symptom improvement including stool frequency and consistency, using symptom diaries, IBS-quality of life (IBS-QoL), and depression and anxiety, at week 4. Results The VAS scores of abdominal pain at week 4, were significantly decreased in both tiropramide and octylonium groups, but the change from baseline did not differ between the 2 groups (difference, -0.26 mm; 95% CI, -4.33-3.82; P = 0.901). Abdominal pain and discomfort assessed using VAS scores, diaries, and IBS-QoL were also improved by both treatments, and the changes from baseline did not differ. The incidence of adverse events was similar in the 2 groups, and no severe adverse events involving either drug were observed. Conclusions Tiropramide is as effective as octylonium in managing abdominal pain in IBS, with a similar safety profile.
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서울 의과대학 (DEPARTMENT OF INTERNAL MEDICINE)
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