Efficacy of Serotonin Type 3 Receptor Antagonist Ramosetron on Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)-Like Symptoms in Patients with Quiescent Inflammatory Bowel Disease: A Randomized, Double-Blind, Placebo-Controlled Trial.
Efficacy of Serotonin Type 3 Receptor Antagonist Ramosetron on Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)-Like Symptoms in Patients with Quiescent Inflammatory Bowel Disease: A Randomized, Double-Blind, Placebo-Controlled Trial.
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DOI:
10.3390/jcm11236882
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发表时间:
2022-11-22
影响因子:
3.9
通讯作者:
Miwa, Hiroto
中科院分区:
文献类型:
--
作者:
Tomita, Toshihiko;Fukui, Hirokazu;Morishita, Daisuke;Mori, Sumire;Oshima, Tadayuki;Shinzaki, Shinichiro;Miwa, Hiroto
Patients with quiescent inflammatory bowel disease (IBD) frequently suffer diarrhea-predominant irritable bowel syndrome (IBS-D)-like symptoms, such as abdominal pain or stool irregularities. Here, we assessed the effect of ramosetron, a serotonin type 3 (5-HT3) receptor antagonist, on IBS-D-like symptoms in patients with quiescent IBD. Seventy patients with quiescent IBD, who met the Rome III diagnostic criteria for IBS-D, were randomly assigned to receive either ramosetron (5 μg; n = 35) or a placebo (n = 35) orally once daily for 4 weeks. The primary endpoint was the responder rate for global assessment of relief from overall IBS-D-like symptoms. The responder rates for relief of abdominal pain/discomfort and improvement of bowel habits were also evaluated. The responder rate for relief from overall IBS-D-like symptoms at the final evaluation point was significantly higher in the ramosetron group (35.5%) than in the placebo group (11.4%) (p = 0.037). The responder rate for improvement of bowel habits was significantly higher in the ramosetron group (38.7%) than in the placebo group (14.3%) (p = 0.028). The reduction of stool frequency was significantly greater in the ramosetron group than in the placebo group (p = 0.044). Ramosetron is effective for relief of overall IBS-D-like symptoms in patients with quiescent IBD.
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影响因子:
29.4
作者:
Kilpatrick LA;Labus JS;Coveleskie K;Hammer C;Rappold G;Tillisch K;Bueller JA;Suyenobu B;Jarcho JM;McRoberts JA;Niesler B;Mayer EA
通讯作者:
Mayer EA
影响因子:
4.6
作者:
Fukui H;Oshima T;Tanaka Y;Oikawa Y;Makizaki Y;Ohno H;Tomita T;Watari J;Miwa H
通讯作者:
Miwa H
影响因子:
3.5
作者:
Lee, K. J.;Kim, N. Y.;Rhee, P. L.
通讯作者:
Rhee, P. L.
DOI:
10.1073/pnas.0804812105
发表时间:
2008-10-28
影响因子:
11.1
作者:
Sokol, Harry;Pigneur, Benedicte;Langella, Philippe
通讯作者:
Langella, Philippe
DOI:
10.1254/jjp.69.205
发表时间:
1995-11-01
期刊:
JAPANESE JOURNAL OF PHARMACOLOGY
影响因子:
--
作者:
MIYATA, K;YAMANO, M;AKUZAWA, S
通讯作者:
AKUZAWA, S