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Effects of Sertralin and Duloxetin in treatment of IBS

Phase 3
Recruiting
Conditions
Irritable bowel syndrome.
Irritable bowel syndrome
Registration Number
IRCT20210420051023N1
Lead Sponsor
Birjand University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
192
Inclusion Criteria

No receiving psychological therapies before entering the study
Not having other structural or functional gastrointestinal disorders at the same time
Not suffering from other organic diseases
Not having psychotic disorder and personality disorder
No risk symptoms such as gastrointestinal bleeding, blood in the stool, fever, weight loss, anemia, nocturnal diarrhea, severe heartburn, etc.,

Exclusion Criteria

Consuming alcohol and substances abuse

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Depression score in Beck questionnaire. Timepoint: First study and 30 days after the start of sertraline and duloxetine. Method of measurement: Beck Depression Inventory.
Secondary Outcome Measures
NameTimeMethod
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