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Cited 13 time in webofscience Cited 16 time in scopus
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Efficacy of DA-9701 (Motilitone) in Functional Dyspepsia Compared to Pantoprazole: A Multicenter, Randomized, Double-blind, Non-inferiority Studyopen access

Authors
Jung, Hye-KyungLee, Kwang JaeChoi, Myung-GyuPark, HyojinLee, Joon SeongRhee, Poong-LyulKim, NayoungPark, Kyung SikChoi, Suck CheiLee, Oh YoungHuh, Kyu ChanSong, Geun AmHong, Su JinSohn, Chong IlJung, Hwoon-YongLee, Yong ChanRew, Jong SunJee, Sam RyongKwon, Joong Goo
Issue Date
Apr-2016
Publisher
KOREAN SOC NEUROGASTROENTEROLOGY & MOTILITY
Keywords
DA-9701 (Motilitone); Dyspepsia; Proton pump inhibitor
Citation
JOURNAL OF NEUROGASTROENTEROLOGY AND MOTILITY, v.22, no.2, pp.254 - 263
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF NEUROGASTROENTEROLOGY AND MOTILITY
Volume
22
Number
2
Start Page
254
End Page
263
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/5071
DOI
10.5056/jnm15178
ISSN
2093-0879
Abstract
Background/Aims The effect of proton pump inhibitors (PPI) in Asian functional dyspepsia (FD) patients has not been well established as in Western countries. DA-9701, a novel prokinetic agent, stimulates gastric emptying and modulates visceral hypersensitivity in vivo and in human studies. This study was conducted to compare the efficacy of DA-9701 with a conventional PPI in mono or combination therapy in patients with FD. Methods In this double-blind, randomized, non-inferiority trial, 389 patients diagnosed with FD using Rome III criteria were allocated among 3 groups: 30-mg DA-9701 t.i.d (means 3 times a day), 40-mg pantoprazole, and 30-mg DA-9701 t.i.d + 40-mg pantoprazole. The primary efficacy end-point was a global assessment of the patient binary response or response on a 5-Likert scale after 4 weeks. Results The global symptomatic improvement was 60.5% in the DA-9701 group, 65.6% in the pantoprazole group, and 63.5% in the DA-9701 + pantoprazole group using a 5-Likert scale at week 4 with no significant difference among 3 groups (P = 0.685). Symptom improvement measured by binary outcome was significantly achieved in each of the 3 groups, but not different among groups. Patients in all treatment groups reported significant improvement in the response rate and symptoms according to FD subtypes and dyspepsia-related quality of life (P < 0.001), but there were no significant differences among the 3 groups. Conclusions DA-9701 improves global and individual symptoms and increases dyspepsia-specific quality of life in patients with FD. The efficacy of DA-9701 monotherapy is comparable with pantoprazole and there is no additive effect with combination of DA-9701 and pantoprazole in patients with FD.
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