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Cold Snare Versus Double Biopsy Polypectomy Technique for Removal of Diminutive Colorectal Polyps

Cold Snare Versus Double Biopsy Polypectomy Technique for Removal of Diminutive Colorectal Polyps: a Prospective Randomized Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01646242
Enrollment
54
Registered
2012-07-20
Start date
2012-07-31
Completion date
2013-06-30
Last updated
2014-10-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polyp of Large Intestine

Brief summary

Most of colorectal polyps founded during colonoscopy are diminutive polyps less than 6 mm. However, complete removal of diminutive polyps is required to prevent tumor recurrence and development of potential interval cancers. Currently, a variety of polypectomy techniques such as hot snare, cold snare, and cold forceps polypectomy are frequently used for the removal of diminutive colorectal polyps. In regard to the completeness of polypectomy, there are few data comparing cold snare polypectomy with cold forceps biopsy technique for removal of diminutive (1-5 mm) colorectal polyps. The aim of this study is to compare cold snare polypectomy with cold forceps polypectomy using double biopsy technique for removal of diminutive colorectal polyps.

Interventions

PROCEDUREremoval of eligible polyps using cold snare polypectomy technique

Snare polypectomy using a mini (10 mm open diameter) size electrosurgical snare without application of electrocautery

PROCEDUREremoval of eligible polyps using double biopsy technique

Cold forceps polypectomy using a standard- capacity forceps with double biopsy technique (two bites per one forceps pass)

Sponsors

Kyunghee University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients over the age of 20 * Informed consent

Exclusion criteria

* Patient undergoing antiplatelets (aspirin, clopidogrel and others) or anticoagulant therapy * Known existing bleeding tendency (thrombocytopenia or prolonged INR) * Inflammatory bowel diseases (Crohn's disease, or ulcerative colitis) * ASA class III or more * Pregnancy * Any condition which, in the opinion of the Investigator, places the patient at unacceptable risk if he/she were to participate in the study

Design outcomes

Primary

MeasureTime frame
Complete histologic polyp eradication rate2 weeks

Secondary

MeasureTime frameDescription
Time taken for polypectomy (complete visual eradication of each polyp)2 weekstime from polyp resection to tissue retrieval
Successful tissue retrieval rate of removed tissues2 weeks
Rates of adverse events4 weeksAdverse events include postpolypectomy bleeding and others (polypectomy syndrome or perforation).
Complete visual polyp eradication rate2 weeks

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026