None listed
Conditions
Interventions
None listed
Sponsors
Korea Institute of Oriental Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Males and females above the age of 20. 2. Those who have no problem communication. 3. Those who have undergone the chronic dyspepsia diagnosis at least six months ago. 4. Dyspepsia, gastritis, gastroesophageal reflux patients. 5. Those who consented to participation in this trial and signed an informed consent statement after listening to clear explanation of this clinical trial's purpose and characteristics.
Exclusion criteria
Exclusion criteria: 1. Those who have a serious disease except for chronic dyspepsia. 2. Those with difficulty imposing a strict restriction on any oral activities (such as eating, brushing teeth, etc.) for at least 4 hours. 3. Pregnant and mental patients. 4. Others who clinical trial conductors consider inappropriate for participating in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Color information of tongue image for using computerized tongue image analysis system (CTAS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of tongue coating and estimation of teethmark by computerized tongue image analysis system (CTAS);Spleen Qi deficiency questionnaire (SQDQ) score ;Nepean dyspepsia index-Korean version (NDI-K) score;Dyspepsia's types for using Rome ? criteria;Halitosis;Fungiform papillae number;Visual Analogue Scale (VAS) of heartburn and epigastralgia;Heart Rate Variability (HRV) | — |
Countries
Korea, Republic of
Contacts
Public ContactJihye Kim
Korea Institute of Oriental Medicine
Outcome results
None listed