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A Randomized Controlled Trial Comparing 7 day Vonoprazan based Triple Therapy and 14 day Omeprazole based Triple Therapy for Helicobacter pylori Infectio

Phase 4
Conditions
Helicobacter pylori infection
Registration Number
TCTR20210219007
Lead Sponsor
Research department, Rajavithi hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Enrolling by invitation
Sex
All
Target Recruitment
120
Inclusion Criteria

1.Present with Helicobacter pylori infection: confirm by one or more of the following methods
-Urea breath test
-Rapid urea test or
- Histology
2. Patient agree to joint the project

Exclusion Criteria

1.history of allergy to PPI, vonoprazan, penicillin , clarithromycin
2. Previous H. Pylori eradication therapy
3. History of antibiotic to effect H. Pylori treatment before 1 month
4. History of GI malignancy or surgery
5. Serious cardiovascular, pulmonary, renal, hepatic disorder or malignancy
6. Pregnancy or lactating
7. History of drug or alcohol abuse

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Eradication rate of H. Pylori infection 4-6 week Eradication success was evaluated by 14C-urea breath test at 4-6 weeks after the completion of treatment
Secondary Outcome Measures
NameTimeMethod
Adverse event of H. Pylori treatment 3 and 14 days adverse reactions listed in the questionnaires were bitter taste, nausea and vomiting, diarrhea, and fatigue
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