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Evaluating the effects of yogurt containing probiotics in treating gastroesophageal reflux disease

Phase 2
Conditions
Gastroesophageal reflux disease (GERD).
Gastro-esophageal reflux disease
Registration Number
IRCT20190831044653N4
Lead Sponsor
Bojnourd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
120
Inclusion Criteria

The patient be literate or someone helps him/her in filling the questionnaires
Patients should be geographically accessible

Exclusion Criteria

Age less than 18 years
Allergy to dairy products
Pregnancy
History of gastrointestinal malignancy
History of gastric and esophageal surgery and small bowel bypass
Liver and kidney and heart dysfunction
Concomitant use of NSAIDs and aspirin for up to one week before the study
Anticancer or antibiotic use during 4 weeks before referral and participation in this study
No anti-acid, hydrogen pump inhibitors, H2 receptor inhibitors in two groups of yogurt recipients during the study
Receiving bisphosphenate, cortisone, potassium chloride or iron tablets concurrently in the study
Patient's compliance be less than 80% (self-reported by patient)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Effect on the GERD severity. Timepoint: Baseline, one month and tow months later. Method of measurement: The Gastroesophageal Reflux Disease-Health Related Quality of Life instrument (related to typical symptoms).;Effect on the severity of GERD atypical symptoms. Timepoint: Baseline, one month and tow months late. Method of measurement: Reflux Symptom Index and Disease Specific Quality of Life Index questionnaires (related to atypical symptoms).
Secondary Outcome Measures
NameTimeMethod
Assessment of quality of life. Timepoint: At baseline, one month and tow months later. Method of measurement: questionnaire.
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