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dc.contributor.authorPham Thi Van Anh, Nguyen Phuong Thanh-
dc.contributor.authorDau Thuy Duong-
dc.date.accessioned2023-02-08T08:57:48Z-
dc.date.available2023-02-08T08:57:48Z-
dc.date.issued2021-
dc.identifier.urihttp://thuvienso.thanglong.edu.vn//handle/TLU/5629-
dc.descriptionSố 148 E9 (12): Tr. 68-77vi
dc.description.abstractA double-blind, randomized, phase II clinical trial was conducted within a 14-week follow-up including 2 weeks of the non-drug run-in period, 8 weeks of medication, and 4 weeks of follow-up after discontinuation. The objective of the study was to evaluate the efficacy and safety of Trang Phuc Linh Plus in irritable diarrhea syndrome patients. Group I took Trang Phuc Linh Plus 3 tablets/time x 2 times/day for 8 weeks; Group II took placebo 3 tablets/ time x 2 times/day for 8 weeks. Patients will be re-examined, tested, and evaluated over the phone for symptom recurrence and adverse events (AEs). This study showed that the Trang Phuc Linh Plus tablets tended to improve symptoms in patients suffering from irritable bowel syndrome with diarrhea, suggesting its safety and tolerabilityvi
dc.language.isoenvi
dc.publisherJournal of Medical Researchvi
dc.subjectirritable bowel syndromevi
dc.subjectTrang Phuc Linh Plusvi
dc.titleEfficacy and safety of Trang phuc linh plus tablets in patients with irritable bowel syndrome-diarrheavi
dc.typeArticlevi
Appears in CollectionsLĩnh vực Khoa học sức khỏe

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