Efficacy and Safety of Black Seed Oil With Vonoprazan Based Triple Therapy in Treatment of Helicobacter Pylori
Helicobacter Pylori Infection
About this trial
This is an interventional treatment trial for Helicobacter Pylori Infection focused on measuring Helicobacter pylori infection, vonoprazan, black seed oil, oxidative stress
Eligibility Criteria
Inclusion Criteria: Male or female patients Age 18 to 75 years old Patients with confirmed H. pylori infection by stool Ag test who had not received prior eradication therapy Exclusion Criteria: History of hypersensitivity / allergy to any of the study drugs i.e., Esomeprazole, vonoprazan, penicillin, or clarithromycin History of previous H. pylori eradication therapy History of using PPIs, antibiotics that affect H. pylori within 4 weeks History of gastric malignancy or surgery Serious cardiovascular, pulmonary, renal, hepatic disorders or active malignancy Pregnancy or breast feeding History of drug abuse or active alcohol abuse
Sites / Locations
- GIT department zagazig university hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Group 1 , Black seed oil group
Group 2 , control group
45 patients will receive they will receive 1800 mg (4 soft gelatin capsules of 450 mg) black seed oil (2 capsules twice daily 30 min after the meal) for 6 weeks plus vonoprazan-based triple therapy ( conventional therapy ) consists of vonoprazan 20 mg twice daily, clarithromycin 500 mg twice daily, and amoxicillin 1000 mg twice daily for 14 days
This group consists of 45 patients, who will receive vonoprazan-based triple therapy(conventional therapy ) consists of vonoprazan 20 mg twice daily, clarithromycin 500 mg twice daily, and amoxicillin 1000 mg twice daily for 14 days