functional gastrointestinal disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients undergoing colonoscopy at the implementing facility
Exclusion criteria
Exclusion criteria: Patients who are pregnant. Patients with serious underlying diseases (serious respiratory disease, cardiac failure, renal failure, hepatic failure). Patients who are considered ineligible by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| At the time of maximum intestinal distension Intra-intestinal pressure (IIP) max Intra-intestinal pressure (IIP) max at the time of maximum intestinal distension Uphill pattern/flat pattern Intestinal pressure waveform slope Endoscopic findings at the time the maximum pressure was recorded Investigate trends in each section (small bowel, cecum to ascending colon, transverse colon, descending colon, sigmoid colon, rectum). | — |
Secondary
| Measure | Time frame |
|---|---|
| Association with factors outside the intestinal tract that may affect intestinal content Association with factors outside the intestinal tract that may affect the intestinal content: body size (height and weight BMI), history of abdominal surgery, inflammatory diseases of the abdomen, etc. Endoscopic findings: association with factors related to intestinal wall extension (e.g., scarring of the intestine) Intra-intestinal pressure changes when intestinal peristalsis is induced Changes in bowel pressure before and after administration of a test drug that has an effect on bowel peristalsis Changes in abdominal symptoms associated with pressurization (non-sedated patients) Assess the relationship between the degree of distress and the pressure at which distress was felt using the VAS scale | — |
Countries
Japan
Contacts
Showa University Koto Toyosu Hospital Digestive disease center