Comparing Cold Biopsy Forceps Versus Cold Snare Biopsy for Colon Polyps
- Conditions
- Colon Polyps
- Interventions
- Procedure: Cold snare biopsyProcedure: Cold Biopsy forceps
- Registration Number
- NCT01665898
- Lead Sponsor
- Incheon St.Mary's Hospital
- Brief Summary
Comparing the efficacy of cold biopsy forceps versus cold snare biopsy for removing colon polyps.
- Detailed Description
Polyps were randomized to be treated with either CSP or CFP. After the initial polypectomy, additional EMR was performed at the polypectomy site to assess the presence of residual polyp tissue.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 138
- patients older than 40 years old and
- patients who are receiving colonoscopies and
- patients who have colon polyps
- patients who have not agreed to the study
- patients with bleeding tendencies
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Cold Snare Biopsy Cold snare biopsy Cold snare biopsy for removal of colon polyps Cold biopsy forceps Cold Biopsy forceps Cold biopsy forceps for removal of colon polyps
- Primary Outcome Measures
Name Time Method Comparing the complete removal rate of cold biopsy forceps versus cold snare biopsy for removing colon polyps up to 3 years We will investigate the complete removal rate of colon polyps by using two different methods, cold biopsy forceps or cold snare biopsy. After removal of polyps by one of these two methods, the remnant lesion will be biopsied to study if there are any remnant tissues in order to find out the complete removal rate.
- Secondary Outcome Measures
Name Time Method Bleeding rate after removal of colon polyps by using cold biopsy forceps or cold snare biopsy participants will be followed up for 1 month We will investigate bleeding rate after removal of colon polyps by these two methods. Bleeding rate will be the number of patients who showed significant bleeding after the procedure divided by the total number of patients who will receive the procedure. Significant bleeding was determined to be ongoing bleeding for more than 30 seconds after the procedure
Trial Locations
- Locations (1)
Incheon St. Mary's Hospital
🇰🇷Incheon, Korea, Republic of