IRCT20210831052349N1
Recruiting
Phase 3
Comparison of the effectiveness of anti-anxiety medication (buspirone and sertraline) on anxiety and gastrointestinal symptoms of functional dyspepsia patients
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Birjand University of Medical Sciences
- Enrollment
- 141
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Willingness to participate in the study after fully explaining the objectives of the research and the disadvantages and advantages of the methods
- •not receiving psychological therapies before entering the study
- •No alcohol and drugs
- •Absence of danger signs such as gastrointestinal bleeding, blood in the stool, fever, weight loss, anemia, nocturnal diarrhea, severe heartburn
- •No psychotic disorder and personality disorder
- •Possibility to keep the type and amount of drug used during the research period if the drug is used
- •No other organic disease
- •Lack of other structural or functional gastrointestinal disorders
Exclusion Criteria
- •Having psychotic disorder or other gastrointestinal disorders
- •Existence of danger signs in the patient (such as gastrointestinal bleeding, blood in the stool, fever, weight loss, anemia, nocturnal diarrhea, severe heartburn, etc.)
- •Having complete criteria for personality disorder
Outcomes
Primary Outcomes
Not specified
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