None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Inclusion criteria Patients who consented to the study among patients undergoing gastric underwater endoscopic mucosal resection from the date of approval of the IRB at the hospital until September 2021
Exclusion criteria
Exclusion criteria: 2)exclusion criteria 1. Patients who disagree with the study 2. Patients who do not undergo gastric underwater endoscopic mucosal resection 3. Under 20 or over 75 4. Patients with the poor general condition [Asia grade (American Society of Anesthesiologists' Physical Status Classification) IV or higher] 5. Patients with an uncontrolled hemorrhagic predisposition 6. Patients with cirrhosis 7. Patients undergoing dialysis 8. Pregnant women 3)withdrawal criteria 1. In case the consent is not obtained and explained properly before the clinical trial 2. When a patient withdraws from the clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Complete resection rate (En bloc resection rate and R0 resection) | — |
Secondary
| Measure | Time frame |
|---|---|
| the secondary goal is to identify adverse events such as bleeding and perforation, average procedure time, amount of water filling the gastric lumen, whether to use additional blood coagulation device such as Coagrasper or Endoclip, whether there are recurrences in the follow-up endoscopy | — |
Countries
Korea, Republic of
Contacts
Chonnam National University Hospital