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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05273697
Other study ID # PN61759
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 21, 2022
Est. completion date July 15, 2023

Study information

Verified date November 2023
Source National and Kapodistrian University of Athens
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Colon cancer is internationally the third cause of deaths from a malignant disease. Screening colonoscopy in adults >45 years of age aims at the early diagnosis and treatment colon polyps that are precancerous lesions. Endoscopic polyp removal (polypectomy) can be done with various techniques depending on the size, morphology, location of the polyp etc. According to updated guidelines, non-pedunculated polyps of small size are treated with a cold snare in air dilated intestinal lumen (conventional cold snare polypectomy - CCSP).In recent years, several studies have described the benefits of water aided colonoscopy, as well as safety and efficacy of underwater polypectomy in large colon polyps. However, there is not enough data on small polyps which are the most commonly diagnosed.This is a prospective randomized double-blind clinical trial to compare the safety and efficacy of CCSP to underwater cold snare polypectomy (UCSP)for non-pedunculated polyps of size of 5-10 mm. A total of 398 polyps will be randomized and randomization will be performed via random numbers method of Microsoft Excel 2016. Primary outcome of this study is to determine muscularis mucosa resection rate. Secondary outcomes are the depth and percentage of R0 excisions and possible complications. The investigators expect UCSP to ensure a higher muscularis mucosa resection rate and they attempt to examine the resection depth in the submucosal layer.These results will provide useful data for the development of guidelines in polypectomy techniques for non-pedunculated polyps 5-10mm.


Recruitment information / eligibility

Status Completed
Enrollment 396
Est. completion date July 15, 2023
Est. primary completion date June 11, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: 1. Age > 20years 2. Non pedunculated polyps (Paris classification Isp, Is, IIa, IIb) 3. Polyp size: diameter of 5 to 10mm 4. Endoscopic diagnosis of mucosal lesions - must not present malignant submucosal infiltration evidence like deepening, ulceration / ulcer, abnormal vessels, irregular surface, (NICE 1, NICE 2A, BASIC) 5. Informed consent 6. Patients who receive antiplatelet / anticoagulant therapy are included in the study only if their therapy has been modified according to ESGE guidelines Exclusion Criteria: 1. Age <20 years old 2. Pedunculated polyps 3. Lesions with macroscopic elements of high-grade dysplasia or submucosal infiltration 4. Sites with previous polypectomy 5. Patients with idiopathic inflammatory bowel disease 6. Patients with coagulation disorders 7. Patients with severe organ failure 7.Patients who during endoscopy will undergo any technique using electrocautery / electrocoagulation will not be eligible for participation in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Underwater Cold Snare Polypectomy
The procedure of Underwater Cold Snare Polypectomy (UP) will be as follows: Complete suction of air from the intestinal tract Partial opening of the intestinal lumen by using sterile room temperature water via a water pump Complete immersion of the lesion in water Snaring of the lesion and a small amount of surrounding healthy tissue (1-2mm) Excision The objective will be the en bloc resection of the lesion including healthy tissue (about 2mm). If the en bloc resection fails, a piecemeal will be performed on as few specimens as possible
Conventional Cold Snare Polypectomy
The procedure of Conventional Cold Snare Polypectomy (CCSP) will be as follows: If the entry during the endoscopy has been made with water, the water will be aspirated, and the intestinal lumen will be re-stretched using air / CO2 Snaring of the lesion and a small amount of surrounding healthy tissue (1-2mm) Excision The objective will be the en bloc resection of the lesion including healthy tissue (about 2mm). If the en bloc resection fails, a piecemeal will be performed on as few specimens as possible

Locations

Country Name City State
Greece Sismanogleio General Hospital Athens

Sponsors (1)

Lead Sponsor Collaborator
National and Kapodistrian University of Athens

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary percentage of muscularis mucosa included in specimen (%) Determination of percentage of muscularis mucosa included in specimen. The determination of the percentage of the area containing muscularis mucosa layer will be done by measuring the length of muscularis mucosa mm / length of specimen mm x100%. Using an ocular and stage micrometer, the length of the muscularis mucosa underlining a neoplastic lesion was measured, along with the specimen's maximum diameter (mm) through study completion, an average of 1 year
Secondary Presence or absence of submucosal in the specimen and its depth (if present) Presence or absence of submucosa
- Measurement of submucosa depth in µm (when submucosa is present in the specimen)
through study completion, an average of 1 year
Secondary Percentage of R0 Resections Vial 1 : Determination of polypectomy margin according to Residual Tumor Classification Vial 1A : Determination of horizontal margins: presence of residual damage or not In order to determine the horizontal margins, 2-4 biopsies will be taken from the resection area (2 biopsies antidiametrically in polyps of 5-7 mm size, 4 biopsies in polyps of 8-10 mm size). One cup of forceps will be placed in the defect and the second in the macroscopically normal mucosa.
The received tissue pieces will be placed in a new vial with formol (Vial 1A)
A microscopically margin-negative resection will be characterized as "R0 resection" The determination of R0 Resection Rate will be done by measuring the number of R0 resections / number of all the resections regardless R classification
through study completion, an average of 1 year
Secondary Complication rate intraprocedural bleeding, post-procedural bleeding, perforation, abdominal pain not due to perforation. These complications will be evaluated by a study physician of the Gastroenterology Department with a phone call and clinical examination if needed 30 days after the polypectomy (treatment procedure)
Secondary Recurrence lesion rate during repeat colonoscopy in 6-12months A subgroup of the sample size will undergo a follow up colonoscopy in 6-12 months in order to identify lesion recurrence 6-12 months after polypectomy (treatment procedure)
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