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Comparing Cold Biopsy Forceps Versus Cold Snare Biopsy for Colon Polyps

Not Applicable
Completed
Conditions
Colon Polyps
Interventions
Procedure: Cold snare biopsy
Procedure: 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
Inclusion Criteria
  • patients older than 40 years old and
  • patients who are receiving colonoscopies and
  • patients who have colon polyps
Exclusion Criteria
  • patients who have not agreed to the study
  • patients with bleeding tendencies

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Cold Snare BiopsyCold snare biopsyCold snare biopsy for removal of colon polyps
Cold biopsy forcepsCold Biopsy forcepsCold biopsy forceps for removal of colon polyps
Primary Outcome Measures
NameTimeMethod
Comparing the complete removal rate of cold biopsy forceps versus cold snare biopsy for removing colon polypsup 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
NameTimeMethod
Bleeding rate after removal of colon polyps by using cold biopsy forceps or cold snare biopsyparticipants 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

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