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dc.contributor.author이오영-
dc.date.accessioned2017-03-10T00:49:23Z-
dc.date.available2017-03-10T00:49:23Z-
dc.date.issued2015-07-
dc.identifier.citationJOURNAL OF NEUROGASTROENTEROLOGY AND MOTILITY, v. 21, NO 3, Page. 414-422en_US
dc.identifier.issn2093-0879-
dc.identifier.issn2093-0887-
dc.identifier.urihttp://www.jnmjournal.org/journal/view.html?doi=10.5056/jnm14117-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/26005-
dc.description.abstractBackground/Aims Therapies of functional dyspepsia (FD) are limited. DA-9701 is a novel prokinetic agent formulated with Pharbitis semen and Corydalis Tuber. We aimed to assess the efficacy of DA-9701 compared with itopride in FD patients. Methods Patients with FD. randomly received either itopride 50 mg or DA-9701 30 mg t.i.d after a 2-week baseline period. After 4 weeks of treatment, 2 primary efficacy endpoints were analyzed: the change from baseline in composite score of the 8 dyspeptic symptoms and the overall treatment effect. Impact on patients' quality of life was assessed using the Nepean Dyspepsia Index (NI) questionnaire. Results We randomly assigned 464 patients with 455 having outcome data. The difference of the composite score change of the 8 symptoms between the 2 groups was 0.62, indicating that DA-9701 was not inferior to itopride. The overall treatment effect response rate was not different between the groups. When responder was defined as ˃= 5 of the 7 Likert scale, responder rates were 37% of DA-9701 and 36% of itopride group. Patients receiving DA-9701 experienced similar mean percentage of days with adequate relief during the 4-week treatment period compared with those receiving itopride (56.8% vs 59.1%). Both drugs increased the NDI score of 5 domains without any difference in change of the NDI score between the groups. The safety profile of both drugs was comparable. Conclusions DA-9701 significantly improves symptoms in patients with FD. DA-9701 showed non-inferior efficacy to itopride with comparable safety.en_US
dc.description.sponsorshipThis study was supported by grant number PF06205-00 from the Plant Diverse Research Center of 21C Frontier R&D Programs, Ministry of Science and Technology, Korea.en_US
dc.language.isoenen_US
dc.publisherKOREAN SOC NEUROGASTROENTEROLOGY & MOTILITYen_US
dc.subjectClinical trialen_US
dc.subjectDA-9701en_US
dc.subjectFunctional dyspepsiaen_US
dc.subjectItoprideen_US
dc.titleRandomized, Controlled, Multi-center Trial: Comparing the Safety and Efficacy of DA-9701 and Itopride Hydrochloride in Patients With Functional Dyspepsiaen_US
dc.typeArticleen_US
dc.relation.no3-
dc.relation.volume21-
dc.identifier.doi10.5056/jnm14117-
dc.relation.page414-422-
dc.relation.journalJOURNAL OF NEUROGASTROENTEROLOGY AND MOTILITY-
dc.contributor.googleauthorChoi, Myung-Gyu-
dc.contributor.googleauthorRhee, Poong-Lyul-
dc.contributor.googleauthorPark, Hyojin-
dc.contributor.googleauthorLee, Oh Young-
dc.contributor.googleauthorLee, Kwang Jae-
dc.contributor.googleauthorChoi, Suck Chei-
dc.contributor.googleauthorSeol, Sang Young-
dc.contributor.googleauthorChun, Hoon Jai-
dc.contributor.googleauthorRew, Jong-Sun-
dc.contributor.googleauthorLee, Dong Ho-
dc.relation.code2015013197-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidleeoy-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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