Functional dyspepsia. Functional dyspepsia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with one of the symptoms of ROME IV dyspepsia criteria lasting at least 6 months and the patient should have these symptoms at least 3 days a week for 3 months: Complaining of postprandial fullness OR complaining of heart burn OR complaining of stomach pain OR complaining of premature satiety willingness to participate in the study by signing the informed consent form
Exclusion criteria
Exclusion criteria: Allergy to zataria and Placebo (corn starch) Diagnosis of organic indigestion before or during the study taking anticoagulants such as warfarin, Plavix, aspirin and other drugs that may interact with zataria or have a possible positive or negative effect on functional indigestion Pregnancy or schedule for it during the study period breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postprandial distress and pain score in Gastrointestinal Symptom Rating Scale (GSRS) questionnaire and Single dyspepsia symptom scale (SDS). Timepoint: Before intervention and 2 weeks after intervention. Method of measurement: Gastrointestinal Symptom Rating Scale (GSRS) questionnaire and Single dyspepsia symptom scale (SDS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Shiraz University of Medical Sciences