Acute bleeding after upper gastrointestinal ESD and EP
Conditions
Interventions
Bleeding group:NA
Non-bleeding group:NA
Sponsors
Peking Union Medical College Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: 1. Aged over 18 but not exceeding 85 years; 2. Patients scheduled to undergo gastric or duodenal ESD or EP treatment; 3. Patients or their family members are able to understand the study protocol and are willing to participate in the study, signing a written informed consent form.
Exclusion criteria
Exclusion criteria: 1. History of abdominal surgery; 2. Presence of gastrointestinal motility disorders or systemic underlying diseases that may cause abnormal gastrointestinal motility; 3. Diseases that may lead to intestinal adhesions, such as cholecystitis or appendicitis; 4. Long-term use of medications affecting gastrointestinal motility; 5. History of psychiatric disorders; 6. Allergy to silicone, 3M dressings, or PC materials; 7. Pregnant or lactating women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occurence of post-upper gastrointestinal ESD and EP bleeding; | — |
Secondary
| Measure | Time frame |
|---|---|
| The lead time provided by bowel sound monitoring for predicting postoperative hemorrhage;Volume of blood transfusion;Length of postoperative hospitalization; | — |
Countries
China
Contacts
Public ContactDong Wu
Peking Union Medical College Hospital
Outcome results
None listed