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Evaluation of the effectiveness of two- and four-drugs regimens in eradication of H pylori

Comparison of the efficacy of 14-days high dose dual therapy and 14 days concomitant regimens as first line regimen for Helicobacter pylori eradication

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20131124015510N5
Enrollment
210
Registered
2022-05-27
Start date
2022-05-22
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Peptic ulcer disease and H pylori infection. Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters

Interventions

Intervention 1: Intervention group: In this study, patients in the intervention group used esmoprazole capsules 40 mg three times a day and amoxicillin 500 mg capsules three times a day for 14 days. I

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: People with peptic ulcer or gastro-duodenal erosion Helicobacter pylori infection on a pathological biopsy or Rapid urease test who have not previously received a Helicobacter pylori eradication regimen

Exclusion criteria

Exclusion criteria: Age under 18 years Pregnancy and lactation Concomitant use of anticoagulants, corticosteroids or ketoconazole atients who have a history of gastric surgery Patients with a confirmed history of severe heart or lung failure, chronic kidney failure, chronic liver disease or a history of cancer. History of drug allergy to the drugs of this study Previous history of Helicobacter pylori eradication

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori infection rat. Timepoint: Evaluation of Helicobacter pylori infection at the beginning of the study and then 8 weeks after receiving the desired treatment regimen. Method of measurement: Measurement of Helicobacter pylori infection variable by pathology at the beginning of the study and confirmation of eradication at the end of the study by fecal antigen method.

Secondary

MeasureTime frame
H pylori infection eradication. Timepoint: initiation of study and 8 weeks after end of treatment. Method of measurement: At the beginning of treatment by pathology and at the end of treatment by fecal antigen of Helicobacter pylori.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Mohammad Valizadeh Toosi

Mazandaran University of Medical Sciences

seyedmohammadv@yahoo.com+98 11 3335 0672

Outcome results

None listed

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