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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04816292
Other study ID # 90/21 S-EB
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 2021
Est. completion date March 2023

Study information

Verified date March 2021
Source Technische Universität München
Contact Christoph Schlag, MD
Phone +49894140
Email christoph.schlag@mri.tum.de
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Colorectal cancer (CRC) has become the third most common malignant tumor and is the second leading cause of cancer related deaths worldwide. Adenomatous polyps of the colon are possible precursor lesions for CRC. Screening for CRC has been shown effective in preventing CRC and related deaths, especially colonoscopy and resection of adenomatous polyps. Currently, for intermediate sized polyps 5 - 19 mm hot snare polypectomy (HSP) with the use of electrocautery is conventionally used, causing relevant adverse events including haemorrhage and postpolypectomy coagulation syndrome, but is safe regarding complete resection of the polyp due to burning effect on residual tissue. On the other hand, cold snare polypectomy (CSP) has grown popularity. Absence of electrocautery makes it technically easier and most important reduces adverse events. CSP is recommended as the preferred technique for polyps <5 mm by the European Society of Gastrointestinal Endoscopy (ESGE) guidelines. In literature, there is one multicenter trial from Japan recommending CSP for polyps 4-9 mm (average polyp size 5,4 mm) and only a few case studies for polyps 10-15 mm with inconsistent results, especially regarding the complete resection and pathological evaluation of the specimen. In this randomized controlled trial, the investigators want to compare the complete resection rates of small and intermediate sized colorectal polyps 5-15 mm with CSP and HSP.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 850
Est. completion date March 2023
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Indication for colonoscopy - at least 1 adenomatous polyp 5-15 mm - provided written informed consent Exclusion Criteria: - American Society of Anaesthesiologists class IV or higher - florid inflammatory bowel disease - emergency indication for colonoscopy - haemorrhagic diathesis - continued dual antiplatelet therapy - continued anticoagulant therapy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Active Comparator: Hot Snare Polypectomy
Hot Snare Polypectomy with the use of electrocautery for the resection of polyps.
Experimental: Cold Snare Polypectomy
Cold Snare Polypectomy without the use of electrocautery for the resection of polyps.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Technische Universität München

Outcome

Type Measure Description Time frame Safety issue
Primary Complete resection rate The histological complete resection rate, determined by pathologically negative margins of the specimen and no residual adenomatous material obtained from two/four biopsies of the resection site. 6 months
Secondary En-bloc resection rate Number of additional resections (snare/forceps) needed. During procedure
Secondary Rate of immediate bleeding with necessity of haemostasis Immediate bleeding: Bleeding >30 seconds after snaring. During procedure
Secondary Rate of impossible resection by CSP An impossible resection by CSP needs electrocautery for successful resection. During procedure
Secondary Time required for resection Time required for resection is the time between the insertion of the snare into working channel to the end of polyp resection. In the HSP group, it is defined as the start of submucosal injection until the end of polyp resection. During procedure
Secondary Rate of procedure-related adverse events. Delayed bleeding, defined as haemorrhage after colonoscopy with the necessity of endoscopic haemostasis. 6 months
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