Defecation disorder
Conditions
Interventions
High dose oligofructose group:40g fructose-oligosaccharide
Low dose oligofructose group:20g dose oligofructose group
Control group:None
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 120 Years
Inclusion criteria
Inclusion criteria: 1. Patients without gastrointestinal surgery; 2. Aged 18 or above; 3. No bowel movement for three consecutive days during the perioperative period; 4. No enema preparation before surgery; 5. Can eat orally, the average daily energy intake >=500kcal; 6. Patients who are informed and agree to participate in this study.
Exclusion criteria
Exclusion criteria: 1. Patients undergoing day surgery; 2. Pregnant or lactating women; 3. Patients with advanced malignant tumor, brain death, and other terminal stage; 4. Patients with obvious gastrointestinal symptoms such as abdominal distension and abdominal pain, or gastrointestinal bleeding; 5. Patients with cognitive impairment and who refused to participate in the study; 6. Patients who are participating in other nutrition research projects; 7. Patients with diabetes, liver and kidney insufficiency, or abdominal distension; 8. Other situations that researchers believe not suitable to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 24 hour defecation rate;Bristol score;Discomfort; | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood glucose 2 hours after oligosaccharides;AST;ALT;CREA; | — |
Countries
China
Contacts
Public ContactFengmei Yu
West China Hospital, Sichuan University
Outcome results
None listed