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Effect of probiotic in intestinal bacterial overgrowth in the irritable bowel syndrome patients

Phase 2
Completed
Conditions
Treatment of Irritable bowel syndrome.
Irritable bowel syndrome
Registration Number
IRCT2013122815959N1
Lead Sponsor
Vice chancellor for research of Ahvaz Jondishapour University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
172
Inclusion Criteria

patients with irritable bowel syndrome based on ROME III criteria and small intestinal bacterial overgrowth based on positive hydrogen breath test. Exclusion criteria: patients with sensitivity to antibiotics, pregnancy, lactation, previous abdominal surgery, past medical history of hypothyroidism, celiac, malignancy, renal and liver insufficiency, diabetes and inflammatory bowel disease, familial history of colorectal carcinoma, ingestion of immunosuppressives and antibiotics in recent 2 months, ingestion of probiotics for more than 2 weeks in recent 6 months.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Expiratory hydrogene. Timepoint: After 10 days treatment with antibiotics and after 3 months treatment with probiotic. Method of measurement: Expiratory hydrogene with micro H2 and hydar hydrogene breath test after ingestion of 1 gram per kilogram body weight glucose in 150 ml water based on ppm.
Secondary Outcome Measures
NameTimeMethod
Incidence of adverse effects of probiotic. Timepoint: At the end of third month of treatment. Method of measurement: Asking from patients.
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