All patients who underwent gastric ESD at our department during the eligible period
Conditions
Interventions
In the first half of the period, the effectiveness of the conventional hemostatic method using hemostatic forceps (number of coagulation hemostasis and size of ulcer base of post-treatment ulcer 1 and
Sponsors
Hiroshima City North Medical Center Asa Citizens Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients who underwent gastric ESD in our department from September 2023 (after Ethics Committee approval) to April 2024 will be included.
Exclusion criteria
Exclusion criteria: Patients who did not give consent for clinical research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the frequency of posterior hemorrhage. Secondary endpoints are the number of coagulation hemostasis at second-look endoscopy and the size of the ulcer base of the posttreatment ulcer at 1 and 2 months after ESD. | — |
Countries
Japan
Contacts
Public ContactNaoki Aaayama
Department of Gastroenterology, Hiroshima City North Medical Center Asa Citizens Hospital, Hiroshima Department of Gastroenterology
Outcome results
None listed