None listed
Conditions
Interventions
Medical Device : This study targets patients with laterally spreading tumors measuring 2 cm or larger. Patients are randomly assigned in a 1:1 ratio to either the T-ESD group or the C-ESD group.
In t
Sponsors
Soon Chun Hyang University Hospital Cheonan
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Adults aged 19 years or older 2) Patients undergoing endoscopic submucosal dissection for a laterally spreading tumor measuring 2cm or larger located in the colon 3) Individuals who, after receiving sufficient explanation about this clinical trial and fully understanding its contents, voluntarily agree to participate and provide written consent to comply with study-related instructions
Exclusion criteria
Exclusion criteria: 1) Elderly individuals aged 80 years or older 2) Cases in which endoscopic submucosal dissection is performed for laterally spreading tumors smaller than 2 cm 3) Cases in which endoscopic submucosal dissection is performed for non-laterally spreading tumor lesions (e.g., ulcer scars, subepithelial lesions, pedunculated polyps) 4) Patients in whom laterally spreading tumor is resected using procedures other than endoscopic submucosal dissection (e.g. endoscopic mucosal resection, surgery, etc) 5) Patients who cannot discontinue antiplatelet or anticoagulant therapy (e.g., aspirin) before the procedure according to guideline recommendations
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Resection speed of the lesion (mm²/min) | — |
Secondary
| Measure | Time frame |
|---|---|
| En bloc resection rate;R0 resection rate;length of hospital stay;Delayed bleeding rate;Perforation rate | — |
Countries
Korea, Republic of
Contacts
Public ContactYunho Jung
Soon Chun Hyang University Hospital Cheonan
Outcome results
None listed