Efficacy of Apium graveolense and Trachyspermum copticum on postprandial syndrome
- Conditions
- Functional dyspepsia.Functional dyspepsia
- Registration Number
- IRCT20150927024228N2
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
18 to 60 year-old patients with functional dyspepsia
Presence of symptoms of postprandial distress syndrome
Pregnancy and Lactation
History of convulsion
Use of chemical and herbal drugs of dyspepsia
Serious diseases like diabetes and cardiovascular diseases
History of gastrointestinal surgery
Severe mental retardation
Drug abuse
Use of anticoagulant drug
History of side effects related to use of herbal or chemical medicines
History of peptic ulcer or gastrointestinal reflux disease
Presence of any structural disorder in endoscopy during the last three months
Presence of irritable bowel syndrome
The patient's unwillingness to continue the study, or unwillingness to signing the concent form
Presence of any alarming sign (severe weight loss, anemia, bloody stool, difficult swallowing
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity assessment of dyspepsia. Timepoint: 4 times: baseline, 2,4 and 8 weeks. Method of measurement: The gastrointestinal severity symptom scale.;Quality of life. Timepoint: 3 times: baseline, 4, 8 weeks. Method of measurement: NDI10 quality of life scale.;Frequency assessment of dyspepsia. Timepoint: 4 times: baseline, 2,4 and 8 weeks. Method of measurement: Rome IV questionnaire.
- Secondary Outcome Measures
Name Time Method Side effects. Timepoint: During 8 weeks study. Method of measurement: Side effects questionnnaire.