None listed
Conditions
Interventions
None listed
Sponsors
Kyung Hee University Oriental Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Participants aged 19-75 (2) Participant diagnosed as GERD (3) Participantwho has symptoms of GERD more than 2 times a week (4) Participant who has no stuructural disease under the Esophagogastroduodenoscopy (5) Participant who has same diagnosis result by 2 Korean Medical doctor (6) Participant who consent voluntarily
Exclusion criteria
Exclusion criteria: (1) Participant who has alarm symptoms(ex. severe dysphagia, hematemesis, severe weight loss) (2) Participant who has past history of gastric tumor (3) Participant who underwent chemotherapy due to cancer during recent 1 month (4) Participant who has ischemic cardiac disease (5) Participant who took the unadequate medicine (6) Participant who take part in the other clinical trial (7) Participant who is impossible to take part in the trial (8) Participant who does not consent the participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The agreement between gold standard(daignosis by 2 Korean doctors) and GERD pattern identification tool | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual analogue scale for GERD symptoms;Korean Gastrointestinal Symptom rating scale (KGSRS);Qi-stagnation questionnaire;Yin-deficiency scale score;Spleen Qi deficiency Questionnaire;Perceived Stress Scale(PSS) | — |
Countries
Korea, Republic of
Contacts
Public ContactGajin Han
Kyung Hee University
Outcome results
None listed