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Comparison of Levofloxacin based quadruple therapy with standard treatment in eradication of helicobacter pylori as first line Therapy

Not Applicable
Conditions
Helicobacter Pylori infection.
Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters
Registration Number
IRCT20171112037420N1
Lead Sponsor
Sabzevar University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
98
Inclusion Criteria

Patients who are performed upper endoscopy and have positive rapid urease test.
Patients with over 18 years of age

Exclusion Criteria

Pregnancy
Allergy to medicent which used this study
Patients were treated helicobacter pylori eradication previously.
lack of willingness to continue the period of treatment
lack of willingness to complete the period of treatment

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Eradication of Helicobacter Pylori infection. Timepoint: 3 weeks after the completion of treatment. Method of measurement: Helicobacter pylori stool antigen test.
Secondary Outcome Measures
NameTimeMethod
Diarrhea. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Nausea. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Headache. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Hiccups. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Skin rash. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Papilation. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Bitter taste. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Neuropathic pain. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Constipation. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Chest stress. Timepoint: During the period of treatment. Method of measurement: Questionnaire.;Vometting. Timepoint: During the period of treatment. Method of measurement: Questionnaire.
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