Evaluation of the effect of pyloricin soft gel on Helicobacter pylori infectio
Not Applicable
Recruiting
- Conditions
- Helicobacter pylori infection.Helicobacter pylori [H. pylori] as the cause of diseases classified elsewhereB96.81
- Registration Number
- IRCT20130211012438N27
- Lead Sponsor
- Barij Research Center of Medicinal Herbs
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Confirmation of Helicobacter Pylori infection by gastroenterologist with the help of a sample of pathology taken in the endoscopy or a positive result of anti-Helicobacter pylori antibodies in the serum sample of patients
Patients with functional dyspepsia or gastroduodenal ulcer have indications of eradication of Helicobacter pylori infection
Exclusion Criteria
A person with advanced chronic disease
Any allergy to the drugs used in the study
Pregnancy or breastfeeding
Substance abuse or alcohol use
Having a history of treatment to eradicate Helicobacter pylori infection
Taking antibiotics or bismuth 4 weeks before entering the study
Constipation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical signs. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Eradication rate of helicobacter pylori. Timepoint: after 1 months from the end of treatment. Method of measurement: stool antigen for helicobacter pylori.
- Secondary Outcome Measures
Name Time Method