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Investigating the effect of moxifloxacin in Helicobacter infection

Comparison of effectiveness of moxifloxacin, amoxicillin and pantoprazole regimen with clarithromycin-based four-drug regimen for eradicating Helicobacter pylori infection

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240128060832N1
Enrollment
246
Registered
2024-02-24
Start date
2024-03-20
Completion date
Unknown
Last updated
2024-03-06

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: Intervention group: Administration of amoxicillin 1000 mg every 12 hours, moxifloxacin 400 mg every 12 hours, and pantoprazole 40 mg every 12 hours for 10 days, followed by pantoprazol

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age above 18 years All patients with PUD, peptic ulcer, non-ulcer dyspepsia and intestinal metaplasia (based on pathology samples) underwent endoscopic evaluation and H. pylori positive confirmation by Rapid urease test (RUT). No previous treatment of H. pylori infection Patient consent to participate in the study

Exclusion criteria

Exclusion criteria: Unwillingness to participate in the study Taking antibiotics or non-steroidal anti-inflammatory drugs (NSAID) in the last 4 weeks Allergy to any of the study drugs A history of gastric surgery or the presence of a serious concurrent disease such as cancer Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Determination of positive or negative Helicobacter infection by fecal antigen test. Timepoint: Helicobacter test before and two weeks after treatment. Method of measurement: Helicobacter pylori fecal antigen.

Secondary

MeasureTime frame
Drug side effects. Timepoint: During treatment and two weeks after treatment. Method of measurement: Registration in the patient's self-report questionnaire.;Acceptance of medication. Timepoint: During treatment and two weeks after treatment. Method of measurement: Registration in the patient's self-report questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir hooshang bavarsad

Ahvaz University of Medical Sciences

a.bavarsad@gmail.com+98 61 3333 4663

Outcome results

None listed

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