Evaluating the efficacy of Bunium persicum on functional dyspepsia.
Phase 2
Recruiting
- Conditions
- Functional dyspepsia.Functional dyspepsia
- Registration Number
- IRCT20210602051471N1
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
Patients between 18 and 60 years old who are suffering from functional indigestion and do not have the exclusion criteria.
Who have consciously signed the consent form.
Exclusion Criteria
Organic gastrointestinal disorders
use of anticoagulant drugs
Serious organic, or mental disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Dyspepsia symptoms severity score. Timepoint: 4 times: With arrival, after 2 , 4 and 8 weeks. Method of measurement: Dyspepsia symptoms severity questionnaire.;Dyspepsia symptoms frequency. Timepoint: 4 times: With arrival, after 2 , 4 and 8 weeks. Method of measurement: Dyspepsia symptoms frequency questionnaire.;Quality of life. Timepoint: 3 times: With arrival, after 4 and 8 weeks. Method of measurement: Dyspepsia quality of life questionnaire.
- Secondary Outcome Measures
Name Time Method Drug side effects. Timepoint: With arrival until the end of follow-up period. Method of measurement: Drug side effects questionnaire.