None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients diagnosed with FD (either epigastric pain syndrome (EPS) or postprandial distress syndrome (PDS)) or IBS via Rome Criteria ? 2) Patients who can steadily visit clinics for the treatment 3) Participants who voluntarily agreed for the study
Exclusion criteria
Exclusion criteria: 1) Patients with organic disease which can induce the dysfunction of gastrointestinal (GI) tract (e.g. central nervous system disease, neoplastic disease, metabolic disease, inflammatory disease on GI tract, or taking medicine influencing the function of GI tract) 2) Patients who received active treatment (e.g. hospitalization for severe symptoms of FGID) within 3 months before visiting outpatient Korean medicine clinic 3) Patients participating in other studies 4) Patients who are considered inappropriate for participating in the study, based on the decision of doctors
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change of scores in questionnaire : Nepean Dyspepsia Index Questionnaire;Change of scores in questionnaire : Functional Dyspepsia Quality of Life Questionnaire;Change of scores in questionnaire : Irritable Bowel Syndrome Quality of Life Questionnaire | — |
Secondary
| Measure | Time frame |
|---|---|
| Pattern identification of patients and extracted features : Standard Tool for Pattern Identification of Functional Dyspepsia | — |
Countries
Korea, Republic of
Contacts
Kyung Hee University