A prospective study to evaluate the efficacy and safety of a new knife in endoscopic treatment for gastric neoplasm
- Conditions
- Neoplasms
- Registration Number
- KCT0005164
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
1. 19 years old or older
2. Diagnosed as adenoma or early gastric cancer and meets the indications for endoscopic resection
3. Where he/she voluntarily signed a written informed consent form after hearing an explanation of the purpose, method, effect, etc. of the study
1. Women of childbearing potential who are unable to use adequate contraception or are pregnant or lactating
2. Past history of gastrectomy
3. When endoscopic resection cannot be safely performed due to hemorrhagic disease or coagulation disorder
4. When the investigator determines that endoscopic resection is impossible
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time differences for endoscopic resection
- Secondary Outcome Measures
Name Time Method Time of marking around the lesion;Number of accessories;Complete resection rate