Helicobacter pylori infection.
Conditions
Interventions
Intervention 1: Intervention group: In addition to standard treatment, patients in this group will also take two herbal medicines, Camellia sinensis (green tea) and Supermint (mint tablets), for one m
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with H. pylori who have a positive written Urea Breath Test or Stool Antigen test result Patients who have not received any anti-H. pylori treatment in the past three months
Exclusion criteria
Exclusion criteria: People who do not have a confirmed test and a written positive H. pylori result. People who have been treated for H. pylori infection in the past Patients who have taken antibiotics for any reason in the past three months. Patients with known allergies to herbal ingredients used in the study (supermint and camellia sinensis) People with severe underlying diseases such as gastrointestinal cancers, advanced liver disease, or kidney failure. Pregnant or breastfeeding women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of people whose anti H.Pylori IgG stool antigen test results changed after treatment. Timepoint: Before starting treatment and after completing the treatment period (one month), 5 cc blood samples and stool samples will be taken from all patients to test for IgG Antibody and Stool Antigen. Method of measurement: Helicobacter pylori antigen determination in feces is performed with a special kit and anti-H.pylori IgG level is measured using ELISA. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyedeh Azra Shamsdin
Shiraz University of Medical Sciences
Outcome results
None listed