Comparison of helicobacter pylori eradication rate with four different quadruple regimens in dyspeptic patients.
Phase 2
- Conditions
- Infection with Helicobacter pylori.Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters
- Registration Number
- IRCT2013010612024N1
- Lead Sponsor
- Vice chancellor for research, Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 270
Inclusion Criteria
Patients with positive rapid urea’s test that confirmed with histological finding of helicobacter pylori infection and chronic gastritis were entered in study.
Persons under 18 years of age at the time of endoscopy; those in the last month or bismuth compounds contain any antibiotics for any illness received; Pregnant and lactating women; people with serious diseases such as congestive heart failure; end-stage renal failure; cirrhosis and psychosis; patients with active gastrointestinal bleeding (upper); previous use of H. pylori eradication regimen and any favism patients were excluded from the study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Eradication of Helicobacter pylori. Timepoint: 6 weeks after end of treatment. Method of measurement: UBT.
- Secondary Outcome Measures
Name Time Method Side effects of treatment. Timepoint: At the time of treatment. Method of measurement: Questionnaire.