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The Efficacy of Bismuth in Helicobacter pylori Eradication

The Efficacy of standard Sequential therapy with Bismuth in Helicobacter pylori Eradication

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250529065965N1
Enrollment
124
Registered
2025-08-10
Start date
2024-04-08
Completion date
Unknown
Last updated
2025-08-19

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

Conditions

Helicobacter pylori. Helicobacter pylori [H.pylori]

Interventions

Intervention 1: Intervention group: Standard treatment (omeprazole capsules produced by Iran Darou Company (20 mg every 12 hours), amoxicillin capsules 500 ml produced by Al-Hawi Pharmaceutical Compan

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with functional dyspepsia or gastroduodenal ulcer who have an indication for eradicating Helicobacter pylori infection Confirmation of Helicobacter pylori infection through pathology results obtained from endoscopy or positive stool antigen test for Helicobacter pylori Minimum age 18 years

Exclusion criteria

Exclusion criteria: Previous eradication of Helicobacter pylori Use of antibiotics, PPIs, or chemotherapeutic agents within the 4 weeks prior to the study Patients with a history of gastrectomy or complicated peptic ulcer Pregnant and nursing women established.Patients with recompensated kidney and heart failure

Design outcomes

Primary

MeasureTime frame
Eradication of Helicobacter pylori infection. Timepoint: After the end of the antibiotic treatment period, omeprazole treatment was continued for 4 weeks, and eradication of the infection was measured two weeks after omeprazole was discontinued. Method of measurement: Fecal antigen test.

Secondary

MeasureTime frame
Side effects of treatment (bitter taste in the mouth, black stool, diarrhea, nausea, vomiting). Timepoint: After the treatment period. Method of measurement: Patient self-expression.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Sadeghi

Kashan University of Medical Sciences

Sadeghi.98.1f@gmail.com+98 31 5500 9999

Outcome results

None listed

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