Skip to content

Comparing success rate of quadruple and triple antibiotic therapy in eradicating H. Pylori infection

Comparing success rate of quadruple and triple antibiotic therapy in eradicating H. Pylori infection in southwest of Iran

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015050622118N1
Enrollment
60
Registered
2015-07-24
Start date
2014-08-25
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Helicobacter. Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters

Interventions

Treatment - Drugs
Intervention 1: Intervention group: quadruple antibiotic regimen include: amoxicillin 1000 mg bid, metronidazol 500 mg bid, bismuth subcitrate 2 tablets bid, pantoprazole 40 mg bid for a two-week peri
Intervention group: quadruple antibiotic regimen include: amoxicillin 1000 mg bid, metronidazol 500 mg bid, bismuth subcitrate 2 tablets bid, pantoprazole 40 mg bid for a two-week period.
Control group: triple antibiotic regimen include: amoxicillin 1000 mg bid, clarithromycin 500 mg bid, pantoprazole 40 mg bid for a two-week period.

Sponsors

Vice Chancellor for research of Yasuj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients aged 15- 80 years; patients with dyspepsia Exclusion criteria: Patients with history of H. pylori eradication treatment;taking antibiotics in the last month; gastrointestinal bleeding; chronic pulmonary, liver or renal diseases; history of gastric surgery; pregnancy; recent consumption of NSAID; taking PPI or H2 receptor antagonists in the previous week

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
H pylori eradication. Timepoint: 6 week after treatment. Method of measurement: Stool H pylori antigen.

Secondary

MeasureTime frame
Drug reaction. Timepoint: Until 6 weeks after treatment. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMoslem Sedaghattalb

Yasuj University of Medical Science

m.sedaghattalab@yums.ac.ir+98 74 3322 0163

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026