The safety and efficacy of colon endoscopic submucosal dissection(C-ESD) using robotic assistance.
- Conditions
- Neoplasms
- Registration Number
- KCT0009663
- Lead Sponsor
- Korea University Anam Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 15
(1)Adults aged between 19 and 80 years old.
(2)Individuals diagnosed with early-stage gastric cancer, where the lesion is well-differentiated and not deeply invasive, indicating no likelihood of regional lymph node metastasis.
(3)Individuals who meet the indications for ESD.
(4)Individuals for whom, in the opinion of the principal investigator, clinical efficacy through ESD is unlikely.
(5)Individuals who have received a detailed explanation of this clinical trial, fully understood it, and voluntarily agreed to participate by signing a written consent form.
(1)Individuals with a pacemaker due to heart disease.
(2)Individuals with any other implanted electronic devices.
(3)Individuals with colon obstruction and bleeding.
(4)Individuals with GFR (glomerular filtration rate) less than 30.
(5)Individuals with inflammatory bowel disease or pregnant women.
(6)Individuals who have undergone gastrointestinal resection or abdominal surgery.
(7)Individuals who refuse to provide informed consent.
(8)Individuals with a history of hypersensitivity reactions to substances used in previous studies or those containing soy or egg components.
(9)Individuals with a systolic blood pressure below 80 mmHg or an oxygen saturation level below 90%.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method