Colonic Polyp Clinical Trial
Official title:
Cold Snare Polypectomy Versus Hot Snare Polypectomy for Diminutive and Small Colorectal Polyps: a Randomized Controlled Trial
Background:The optimal technique for removal of diminutive or small colorectal polyps is
debatable.
Objective:To compare the complete resection rates of cold snare polypectomy (CSP) and hot
snare polypectomy (HSP) for the removal of adenomatous polyps(3-9mm).
Design:Prospective randomized controlled study. Setting:Three tertiary referral hospitals.
Patients:we will recruit a total of 330 polyps(3-9mm). Interventions:Enrolled patients were
randomly assigned to one of the two polypectomy protocols (CSP vs. HSP) using a
computer-generated random sequence. If a patient had one or more polyps, all eligible polyps
were removed using the initially assigned polypectomy protocol. After the initial
polypectomy, additional EMR was performed at the polypectomy site to assess the presence of
residual polyp tissue.
Main Outcome Measurements:The primary study outcome was to compare the complete polyp
resection rate between groups. Secondary outcomes included rate of postpolypectomy adverse
events, including bleeding, perforations,infection and rate of tissue retrieval(Complete
resection was defined as the absence of residual polyp tissue in the EMR sections of the
polypectomy site).
1、study objective and Contents
Study objective:
Compare cold snare polypectomy with cold forceps polypectomy with respect to their efficacy
and safety for endoscopic resection of small colorectal polyps: a randomized controlled
trial.
Study content:
1. Main Outcome Measurements: The primary study outcome was to compare the complete polyp
resection rate between groups. Secondary outcomes included rate of postpolypectomy
adverse events, including bleeding, perforations,infection and rate of tissue
retrieval(Complete resection was defined as the absence of residual polyp tissue in the
EMR sections of the polypectomy site).
2. Collect the pre-operation and post-operation data of patients who underwent a
colonoscopy in the digestive disease center of Wulumuqi General Hospital of Lanzhou
Militery Cammand from December 2015. to December 2016.Collect patients clinical
data,Laboratory examination data, baseline data.
2、Key technical indicators and Solutions
1. key technique: After each polypectomy, additional EMR was performed at the polypectomy
site, including an additional 1 to 2 mm clear margin, was resected by the snare,to
evaluate for the presence of residual polyp tissue.
2. the implementation of colorectal polypectomy: the polypectomy will be performed by
experienced clinician, our Department of Gastroenterology and Hepatology has conducted
nearly thousand colorectal polypectomy,and is a national leader in this technology. All
the operation done by our team, all the members of our team has been trained to operate
according to the operation standardization.All points mentioned above can ensure the
smooth implementation of the operation.
3、Research methods and technical routes to be used
1. The study was a multicenter, prospective,single-blind, randomized controlled study
involving patients who underwent a colonoscopy from February 2016 to December 2016. It
was conducted according to the Declaration of Helsinki Principles and was approved by
the institutional review board of our hospital (2016LL001). The study was reported
according to the CONSORT guidelines and was registered at www.clinicaltrials.gov.
Written informed consent for this study was obtained from all patients.
2. Patients: Patients come to the digestive disease center of Wulumuqi General Hospital
between 2016.02-2016.12 Inclusion criteria:
(1)patients aged >18 years who undergo a screening, surveillance, or diagnostic colonoscopy
and are subsequently found to have colorectal polyps measuring 3-9 mm in size.(2) Patients
who signed an informed consent.
Exclusion criteria:(1)patients taking antiplatelet or anticoagulant therapy during the past 1
week of the procedure;(2) known coagulopathy;(3) history of inflammatory bowel
diseases;(4)polyposis syndrom;(5)Type IV shantian colorectal polyps;(6)American Society of
Anesthesiology class III or more;(7) pregnancy;(8)Unable to provide informed consent.
(3)Random method: Enrolled patients were randomly assigned to one of the two polypectomy
protocols (CSP vs. HSP) using a computer-generated random sequence. If a patient had one or
more polyps, all eligible polyp swere removed using the initially assigned polypectomy
protocol. (4)data collection:Laboratory data and previous colonoscopy data.Preoperative
baseline data included:Patient entry sequence number,Operation method(CSP or HSP),age,gender,
take anticoagulant drugs or not(Warfarin , aspirin, clopidogrel), cause of desease, operation
indications(Screening, inspection, polypectomy, fecal occult blood test positive, perianal
rectal bleeding, other); Correlation check: 1.Blood routine, urine routine, stool routine +
Occult Blood; 2,Liver and kidney function, electrolyte, blood sugar, blood coagulation, blood
type, Rh factor, infection disease screening (hepatitis B, hepatitis C, HIV, syphilis and
other); 3.Digestive tract tumor marker screening (CA19-9, CA24-2, CEA, etc.); 4.Abdominal
ultrasound, electrocardiogram, chest X-ray. The postoperative data were: Bowel preparation
(using the Boston Bowel Preparation Scale),Whether to insert the coloscope to the cecum, time
of insertion,Whether to send the coloscope to the terminal ileum,Time from the insertion of
the coloscope to thececum to Exit the colonoscope. Total time from the insertion of the colon
to the exit of the colonoscopy.The number of polyps (per patient), polyp size (mm),
anatomical (cecum, ascending colon, transverse colon, hepatic flexure, splenic flexure,
descending colon, sigmoid colon, rectum), shape (flat, sessile,pedunculated ) , the number of
polyps resected, Whether the naked eye view (NBI) is completely removed, the total operation
time,whether the polyps were retrieved, postoperative hemorrhage (postoperative bleeding,
hematochezia, delayed bleeding), Whether or not perforate, whether the use of hemostatic clip
( number), pathological diagnosis (tubulovillous adenoma, sessile serrated adenoma,
hyperplastic polyp and other non neoplastic polyps), whether the additional EMR success after
polypectomy, EMR operation time, the pathological results of EMR tissues (normal intestinal
mucosa,tubulovillous adenoma, sessile serrated adenoma, Hyperplastic polyps, other non
neoplastic polyps), whether the histological complete resection.
(5) Operation procedure:①Bowel preparation consisted of patients drinking a total of 4 L of
polyethylene glycol solution before their procedures.Until the discharge of clean liquid
(colorless or yellow transparent water samples). ②Total colonoscopies were prospectively
performed by using a high-definition endoscope (CF-H260AL; Olympus Co, Tokyo, Japan) by 7
highly experienced endoscopists. All polyps found during colonoscopy were photographed, and
their characteristics, including size,shape and anatomic location, were documented. The size
of the polyp was assessed with the width of the biopsy forceps before the polyps were
removed. ③Polyps that were deemed neoplastic (vessels surrounding oval, tubular, or branched
pits under observation by high-definition white-light endoscopy and narrow-band imaging
endoscopy) were subjected to polypectomy. Polyp size was defined by using the opening width
of the biopsy forceps. If the size of the polyp was eligible for the study (3-9mm),
polypectomy was performed by one of two randomized methods.④ Two kinds of operation methods
are adopted: 1.CSP was performed by using a disposable oval snare with a diameter of 10 mm
(SD-210U-10; Olympus) under gentle suction to reduce colon wall tension. The tip of the
endoscope was deflected toward the polyp base to ensnare 1 to 2 mm of normal mucosa
surrounding the polyp.2.HSP, which is using electrocoagulation on the basis of using cold
snare.⑤After the polyps were removed, the ulcers were washed with saline lavage fluid. After
that, another independent endoscopic surgeon judged whether the endoscopic eradication was
successful. ⑥Afterward, additional EMR was performed at the polypectomy site to evaluate for
the presence of residual polyp tissue.For histologic assessment of residual polyp tissues,
the polypectomy site, including an additional 1 to 2 mm clear margin, was resected by the
snare and Endocut current (VIO300D; Erbe Elektromedizin GmbH, Tubingen, Germany) after
submucosal injection of a mixed solution (normal saline solution + 0.01% epinephrine). In the
event that no tissue could be removed (e.g., if the original resection achieved a wide
resection), or if EMR failed to get in situ mucosal specimens. At least four cold biopsies
using forceps on the remaining margins were obtained. The primary polyp specimen and the
specimen from the base of the polyp were placed in separate jars.⑦After each procedure, the
polypectomy site was observed for 30 seconds to confirm the absence of immediate bleeding,
the specimens were retrieved and stored in formalin.⑧The retrieved specimen was fixed on a
plate by using pins. After indigo carmine solution was applied, the specimen was studied
under a stereomicroscope with 8-power magnification to assess the presence of residual tissue
by the endoscopist who performed the polypectomy. The presence of residual tissue was
documented, and the plate was marked with a pen to indicate the most probable site of
residual tissue. Cross-sections of the EMR specimens were collected at 1-mm intervals;
accurate tissue section of the marked site was ensured. ⑨All tissue samples were
cross-reviewed by 2 experienced pathologists who were blinded to the clinical information.
Histological identification was carried out and the comprehensive analysis was carried out.
The process is shown in Figure 1. ⑩The patients returned 1 week after each polypectomy to be
informed of their pathology results and to be assessed for postprocedural adverse events,
such as delayed bleeding. Complete resection was defined as the absence of residual polyp
tissue in the EMR sections of the polypectomy site.
(6)Statistical analysis: card square test and Fisher exact test were used to compare
categorical variables, the p value less than 0.05 was considered statistically significant,
between groups of continuous variables and discrete variables were compared with a two sample
t test, or Z test. All the data analysis by SPSS windows system.
(7)sample size estimation: according to Hyun-Soo Kim et al: a randomized controlled study of
an GASTROINTESTINAL ENDOSCOPY: cold snare versus hot snare polypectomy for the complete
resection of 5-9 mm sized colorectal polyps; a randomized controlled trial, according to the
CSP with HSP complete resection rate was (79.1% vs 92.2%), the alpha value of the significant
level of 0.05, grasp the degree 1 beta 0.9, according to pass (11.0) software calculated
sample size for 300 cases. Taking into account the possible 10% of the rate of loss of
access, sample size of 330 cases.
Cold snare polypectomy (CSP) has been shown to be safe and effective for the removal of
polyps ≤10 mm in size, and is regarded as the ideal procedure for removal of small polyps.
Hot snare techniques for diminutive polypectomy are still popular, but their use has
decreased steadily in practice because of limited effectiveness and several drawbacks
associated with the use of electrocautery,such as inadequate histologic interpretation and
significant risk of complications. However, there have been few randomized controlled trials
demonstrating complete resection rate by CSP or HSP for diminutive and small polyps. There
are a paucity of data regarding which polypectomy technique is recommended according to polyp
size and shape. The polypectomy techniques in the removal of small colorectal polyps in the
3-9 mm size range are not consistent. The study aimed at the direct comparison of the
histologic polyp eradication rate of cold snare polypectomy (CSP) with that of hot snare
polypectomy (HSP) in 3-9 mm sized flat or sessile colorectal polyps and the efficacy and
safety of CSP to HSP in the removal of polyps 3-9 mm in size. In order to guide clinical
practice.
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