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Compare seven and ten days quadruple regimen for H. pylori

The comparison between effects and side effects of seven days or ten days quadruple therapy regimens (Bismuth sub citrate, Levofloxacin, Amoxicillin and Pantazole) in eradication of H.pylori infection.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201406141155N19
Enrollment
220
Registered
2015-07-10
Start date
2015-07-15
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 infection. Helicobacter pylori [H. pylori] as the cause of diseases classified to other chapters

Interventions

Intervention 1: Administration of quadruple therapy for seven days as follows: Bismuth sub citrate (Chemidarou company) 240 mg BID, Levofloxacin (Abidi company) 500 mg daily, Amoxicillin (Chemidarou
Treatment - Drugs
Administration of quadruple therapy for seven days as follows: Bismuth sub citrate (Chemidarou company) 240 mg BID, Levofloxacin (Abidi company) 500 mg daily, Amoxicillin (Chemidarou company) 1 g B
Administration of quadruple therapy for ten days as follows: Bismuth sub citrate (Chemidarou company) 240 mg BID, Levofloxacin (Abidi company) 500 mg daily, Amoxicillin (Chemidarou company) 1 g BID

Sponsors

Vince Chancellor for Research Guilan University of Medical Sciences .
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: H. pylori infection has been confirmed in accordance with Urea Breath Test with carbon-13 or 14 or pathology or stool antigen, The patient satisfaction Exclusion criteria: Pregnant and lactating women, Patients with esophageal cancer, Liver cirrhosis, Heart failure; kidney failure, History of seizures, Hematologic diseases; Allergy to drugs, Patients with an incomplete course of treatment; Severe complications; Discontent to treatment

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Eradication of infection. Timepoint: Eight weeks after completion of treatment. Method of measurement: Urea breath test (Carbon 14).

Secondary

MeasureTime frame
Complications. Timepoint: Two weeks after completion of treatment. Method of measurement: According to the case history.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJoukar Farahnaz

Guilan Gastrointestinal and Liver Diseases Research Center

info @gldrc.org+98 13 3353 5116

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 10, 2026