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Sequential therapy versus the best quadriple drug therapy for helicobacter pylori eradication

Sequential therapy versus the best quadriple drug therapy for helicobacter pylori eradication

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138807022499N1
Enrollment
296
Registered
2010-02-06
Start date
2009-03-21
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

Peptic Ulcer Disease (H. Pylori eradication). Duodenal ulcer

Interventions

Intervention 1: Intervention group: Pantoprazole 40mg (BD) for 10 days + Amoxicillin 1g (BD) just during the first 5 days + Clarithromycin 500mg (BD) and Tinidazole 500mg (BD) just during the second
Treatment - Drugs
Intervention group: Pantoprazole 40mg (BD) for 10 days + Amoxicillin 1g (BD) just during the first 5 days + Clarithromycin 500mg (BD) and Tinidazole 500mg (BD) just during the second 5 days
Control group: Pantoprazole 40mg (BD) + Amoxicillin 1g (BD) + Bismuth 240mg (BD) for 2 weeks and Furazolidone 200mg (BD) just during the first week

Sponsors

Vice Chancellor For Research, Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age more than 18 years Exclusion criteria: Previous history of receiving any H.p eradication regimen, Taking H2 blocker, proton pump inhibitor, Bismuth or Antibiotics during the 2 weeks prior to the study, Taking anticoagulants, ketoconazole or corticosteroids, History of gastric or esophageal surgery, Severe cardiovascular, pulmonary or endocrine disease, Renal failure, Hepatic diseases, Malignancies, Alcoholism, G6PD deficiency, Pregnancy or breast feeding

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori eradication. Timepoint: 2 months after the completion of treatment course. Method of measurement: urease breating test.

Secondary

MeasureTime frame
Side effects of drugs. Timepoint: daily recording during and after the treatmen course. Method of measurement: classifying as mild, moderate or severe side effects.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Hafez Tirgar Fakheri

Mazandaran University of Medical Sciences

Hfakheri@mazums.ac.irfakheri42@yahoo.com+98 15 1226 1700

Outcome results

None listed

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