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Effect of the Ouji (Menta aquatica) product on bloating

Phase 3
Conditions
bloating.
Abdominal distension (gaseous) Bloating Eructation Gas pain Tympanists (abdominal)(intestinal)
Registration Number
IRCT20190425043371N1
Lead Sponsor
Sari University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

All patient with bloating in basis of IBS 20 - 80

Exclusion Criteria

diabet?heart? liver? kidney failure?asthma?COPD?neoplasm?sever mental disorder
Pregnant women, Women who intend to get pregnant and lactating women
Patients who have had gastric or intestinal surgery
History of receiving drugs to eradicate Helicobacter pylori in the last three months
Alcohol or opioid adiction
People with history of lactase deficiency
Patients who use a cardiovascular medicine, antihypertensive drug, anticoagulants, anxiolytics or steroids.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intensity of bloating. Timepoint: Measure the severity of bloating before starting the study.14 and 28 days after taking Ouji And 14 days after the study. Method of measurement: visual analog scale.
Secondary Outcome Measures
NameTimeMethod
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