None
Conditions
Interventions
Group A:If patients were enrolled in group A, they did not receive rubiprostone. On the day before the examination (breakfast, lunch and dinner), dietary restriction was carried out, only low-residue
Group B:If the patients were enrolled in group B, they were required to eat a low-residue diet from the day before the examination (breakfast, lunch, and dinner), take 1 rubiprostone soft capsule at 1
Group C:If the patients were enrolled in the C group, they were required to eat a low-residue diet from the day before the examination (breakfast, lunch, and dinner), take 1 rubiprostone soft capsule
Sponsors
Ningbo Medical Centre Lihuili Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.18-75 years old, male or female; 2. Planned to undergo diagnostic, screening, or surveillance colonoscopy; 3. Written informed consent was obtained;
Exclusion criteria
Exclusion criteria: 1.severe cardiac, cerebral, pulmonary, or renal complications or acute myocardial infarction within 6 months; 2.Pregnant and lactating women; 3.Stool Bristol score of 7 (watery, no solid mass), considered diarrhea; 4.Had participated in other interventional clinical trials within 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Boston score for bowel preparation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse reactions of bowel preparation;Time to complete bowel preparation;Tolerability of laxatives; | — |
Countries
China
Contacts
Public ContactFeng Xu
Ningbo Medical Centre Lihuili Hospital
Outcome results
None listed