Skip to content

Eradication of Helicobacter pylori infection by sequential regimen and standard quadruple

Comparison of sequential regimen with standard quadruple therapy on eradicating of Helicobacter pylori infection

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
IRCT
Registry ID
IRCT20191007045022N1
Enrollment
160
Registered
2019-10-19
Start date
2018-08-23
Completion date
Unknown
Last updated
2019-11-05

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] as the cause of diseases

Interventions

Intervention 1: Intervention group for the first group: first week: omeprazole (20mg / BD) + amoxicillin (1gr / BD) and second week: omeprazole (20mg / BD) + thinidazole (500 mg / BD) + levofloxacin (

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 with indication of eradication of Helicobacter pylori infection Ability and willingness to participate in study and to give informed consent Verification of Helicobacter pylori infection by endoscopic pathological specimen

Exclusion criteria

Exclusion criteria: Previous eradication of Helicobacter pylori Use of antibiotics, PPI or chemotherapy during 4 weeks prior to study Patients with a history of gastrectomy or Complicated Peptic Ulcer. Pregnant and lactating women Patients with renal failure and heart failure

Design outcomes

Primary

MeasureTime frame
Fecal antigen reduction. Timepoint: Helicobacter pylori eradication was assessed at least 2 months after the end of antibiotic treatment and at least 2 weeks after omeprazole discontinuation via fecal antigen. Method of measurement: Fecal testing.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMayam Madani

Kashan University of Medical Sciences

madani-m@mail.Kaums.ac.ir+98 31 5550 0111

Outcome results

None listed

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