None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Adult men and women 19 years of age or older 2) Signed written informed consent after receiving an explanation of the purpose and methods of the study 3) Irritable bowel syndrome according to Rome IV criteria
Exclusion criteria
Exclusion criteria: 1) Under the age of 19 2) Subjects who do not consent to participate in the study 3) Past history of abdominal surgery (except appendectomy, cesarean section) 4) Patients with inflammatory bowel disease, major psychiatric disorders and those taking medication for depression 5) Subjects with severe cardiopulmonary disease and malignant tumors 6) Taking antibiotics or probiotics or undergoing a fecal transplant within 2 weeks of study enrollment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change of IBS Symptom Severity assessed with the IBS Severity Scoring System (50 points or more decrease) | — |
Secondary
| Measure | Time frame |
|---|---|
| Change of abdominal pain Severity assessed with the IBS Severity scoring System (10 points or more decrease);Change of Irritable Bowel Syndrome Quality of Life Score (10 points or more decrease) | — |
Countries
Korea, Republic of
Contacts
Hallym University Medical Center-Kangnam