Clinical study of H. pylori molecular diagnostic POCT kit.
Not Applicable
- Conditions
- Helicobacter pylori infection
- Registration Number
- JPRN-UMIN000045893
- Lead Sponsor
- MIZUHO MEDY Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who meet any of the following conditions (1) Patients who did not obtain sufficient samples for the study (2) Patients who have already received H. pylori eradication treatment (3) Patients with serious disabilities (4) Pregnant or potentially pregnant patients (5) Other patients who the attending physician has determined to be unable to participate in the study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method For H. pylori molecular diagnostic kit using stool, evaluation of the correlation with H. pylori conventional diagnostic method (urea breath test, stool antigen test, culture) and evaluation of the concordance with clarithromycin antibiotic susceptibility test.
- Secondary Outcome Measures
Name Time Method