A randomized study comparing moxifloxacin, omeprazole, nitazoxanide, and doxycycline versus classic triple therapy for the eradication of helicobacter pylori / Ahmed Bahaa Eldin Abbas ; Supervised Maissa Elsaid Elraziky , Mohammad Elsayed Soliman , Walied Khalid Alhossary
Material type:
- دراسة عشوائية تقارن بين الموكسيفلوكساسين والاوميبرازول والنيتازوكسانيد و الدوكسيسيكلين مقابل العلاج الثلاىى الكلاسيكى في علاج البكتيريا الحلزونيه [Added title page title]
- Issued also as CD
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.33.M.Sc.2019.Ah.R (Browse shelf(Opens below)) | Not for loan | 01010110080130000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.33.M.Sc.2019.Ah.R (Browse shelf(Opens below)) | 80130.CD | Not for loan | 01020110080130000 |
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Tropical Medicine
Introduction:Helicobacter pylori infection is a global concern with rising antimicrobial resistance and declining cure rates which has led to an increased demand for a more efficacious, yet tolerable, therapy. Aim: To evaluate the efficacy and safety of the two regimens (Amoxicillin, clarithromycin and omeprazole for 14 days vs moxifloxacin, doxycycline, nitazoxanide and omeprazole for 14 days) as a first-line treatment for Helicobacter pylori (H. pylori) infection. Patients &Methods: From September 2018 to April 2019, 90 patients with confirmed H. pylori infection were randomized into two groups.The First group (triple group)(n = 44) received amoxicillin 1000 mg, clarithromycin500 mg and Omeprazole 40 mg twice a day for 14 days, the Second group (MOND group) (n = 46) received Moxifloxacin 400 mg, Doxycycline 100 mg once daily, Nitazoxanide 500 mg and Omeprazole 40 mg twice a day for 14 days. Successful eradication of H. pylori infection was defined as a negative Stool antigen test 6 weeks after the end of treatment. Patient compliance was defined as 2good3 if drug intake was at least 90%.Follow up of patient'sadherenceto treatment, adverse event rates and dyspepsia improvement was done 6 weeks after theend of treatment
Issued also as CD
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