Overview

Sequential Therapy Versus Quadruple Therapy in H. Pylori Eradication

Status:
Unknown status
Trial end date:
2019-12-01
Target enrollment:
0
Participant gender:
All
Summary
The investigators aimed to 1. compare the eradication rates and long term re-infection rates of sequential therapy for 14 days versus bismuth quadruple therapy for 10 days in the first line and second line treatment 2. assess the impact of antibiotic resistance and CYP2C19 polymorphism on the eradication rate of these regimens 3. assess the impact of these eradication regimens on the antibiotic resistance and microbiota of the gut flora 4. assess the impact of eradication therapy on the metabolic factors
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
National Taiwan University Hospital
Collaborators:
Chiayi Christian Hospital
E-DA Hospital
Kaohsiung Medical University
Mackay Memorial Hospital
National Taiwan University Hospital Hsin-Chu Branch
Taipei Veterans General Hospital, Taiwan
Treatments:
Bismuth
Criteria
Inclusion Criteria:

1. H. pylori infected patients naïve to eradication therapies will be eligible in this
study.

Exclusion Criteria:

1. children and teenagers aged less than 20 years,

2. history of gastrectomy,

3. gastric malignancy, including adenocarcinoma and lymphoma,

4. previous allergic reaction to antibiotics (bismuth, amoxicillin, metronidazole,
clarithromycin, tetracycline) and PPI (esomeprazole),

5. contraindication to treatment drugs,

6. pregnant or lactating women,

7. severe concurrent disease,

8. concomitant use of clopidogrel, or (9) Unwilling to accept random assignment of
subjects