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Evaluation of treatment success rates in 10-day sequential therapies compare with 14-day standard therapy for Helicobacter pylori

Evaluation of treatment success rates in 10-day sequential therapies compare with 14-day standard therapy for Helicobacter pylori

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014042817474N1
Enrollment
100
Registered
2015-02-28
Start date
2014-08-06
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 pylori. Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters

Interventions

Intervention 1: Trial group treated with pantaprazole once a day for five days and amoxicillin 1 g twice a day and next 5 days they treated with the same dose of pantaprazole and levofloxacin 500 mg d
Treatment - Drugs
Trial group treated with pantaprazole once a day for five days and amoxicillin 1 g twice a day and next 5 days they treated with the same dose of pantaprazole and levofloxacin 500 mg daily and tinidaz
group II (control) treated with pantaprazole 40 mg daily, clarithromycin 500 mg twice a day and amoxicillin 1 g twice a day and metronidazole 500 mg twice a day for 14 days.

Sponsors

Vice chancellor for research,Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients over seventeen years, admitted to the infectious diseases clinics in Firoozgar hospital; the presence of H. pylori in the presence of gastritis or peptic ulcer specimens obtained by endoscopy and rapid urease test. Exclusion criteria: pregnant or lactating women; having chronic illness, such as cancer ( Especially gastrointestinal cancer ) , liver and kidney failure; positive history of antibiotic use in the two weeks prior to admission; no history of allergy to the antibiotics studied.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Urease Breath Test. Timepoint: one month after finishing of treatment. Method of measurement: The presence of H. pylori in the stomach by using carbon 13-labeled urea fed to the patient and the patient's breathing carbon measurement.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Daneshbodi

Medical university of Iran university

marziehdaneshbodi@yahoo.com+98 21 5547 2157

Outcome results

None listed

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