Colorectal polyp
Conditions
Interventions
Experimental Group 1:Initiating oral intake at 6 hours post-procedure
Experimental Group 2:Initiating oral intake at 12 hours post-procedure
Control Group:Initiating oral intake at 24 hours post-procedure
Sponsors
Drum Tower Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.Aged 18-75 years, regardless of gender; 2.diagnosed with colorectal polyps measuring 20-50 mm in diameter; 3.meeting the indications for EMR/ESD; 4.patients voluntarily participate in this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Concomitant gastroesophageal reflux disease or other colorectal disorders; 2.cirrhosis or coagulopathy with a bleeding tendency; 3.undergoing anticoagulant therapy prior to surgery; 4. previous history of colorectal surgery; 5. currently participating in other clinical studies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of Post-procedural Hemorrhage; | — |
Secondary
| Measure | Time frame |
|---|---|
| Total medical costs;Postoperative abdominal pain score;Hospitalization duration;Incidence of Postoperative delayed perforation; | — |
Countries
China
Contacts
Public ContactChen Min
Drum Tower Hospital
Outcome results
None listed