Efficacy of EndoClot™ Spraying After Endoscopic Resection of Large Colorectal Polyps (EndoClot™)
Primary Purpose
Wound Endoscopical, Colon, After Polyp Resection, Colon
Status
Terminated
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
use of EndoClot
Sponsored by
About this trial
This is an interventional prevention trial for Wound Endoscopical, Colon focused on measuring colon endoscopic mucosa resection (EMR), delayed bleeding, colonoscopy, polyp resection
Eligibility Criteria
Inclusion Criteria:
- Patients with a ≥20mm colon non-pedunculated polyp who are undergoing an ESD or EMR resection
- signed Informed Consent
Exclusion Criteria:
- Patients with known (biopsy proven) or strongly suspected invasive carcinoma in a potential study polyp
- Pedunculated polyps (as defined by Paris Classification type Ip or Isp)
- ulcerated depressed lesions (as defined by Paris Classification type III)
- polyposis syndromes
- inflammatory bowel disease
- emergency colonoscopy
- Poor general health (ASA (American Society of Anaesthesiologists) class>3)
- Patients with coagulopathy with an elevated International Normalized Ratio (INR )≥1.5, or platelets <50
- Poor bowel preparation
- pregnancy or breastfeeding
- Intervention planned using ORISE™ (Boston Medical) or LIFTUP™ (Ovesco) as lifting agents
Sites / Locations
- Vivantes Auguste-Viktoria-Klinikum
- University Hospital Hamburg Eppendorf
- Evangelisches Amalie Sieveking Krankenhaus
- UKGM Marburg, Klinik für Gastroenterologie
- Klinikum Südstadt Rostock
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
EndoClot group
Control group
Arm Description
patients who are being provided with EndoClot adhesive spray after polyp resection
no further prophylactic bleeding prevention after polyp resection
Outcomes
Primary Outcome Measures
delayed bleeding complication: hospitalization
hospitalization after subsequent return to unit / health care facility for evaluation of rectal bleeding
delayed bleeding complication: transfusion
a patient who subsequently had to return to the unit and/or any health care facility for evaluation of rectal bleeding AND who required transfusion
delayed bleeding complication: repeat endoscopy
a patient who subsequently had to return to the unit and/or any health care facility for evaluation of rectal bleeding AND who required a repeat colonoscopy or sigmoidoscopy for examination of the polypectomy site or control of bleeding
delayed bleeding complication:
a patient who subsequently had to return to the unit and/or any health care facility for evaluation of rectal bleeding AND who required surgery
Secondary Outcome Measures
Technical handling
product deployment assumed quantity of entire vial: < 50%/50-70%/100%
Overall complications
an aggregate of all complications that occur at the time of the procedure or during follow-up
Factors associated with complications: polyp size
Factors that may be associated with complications, esp. bleeding
Factors associated with complications: polyp location
Factors that may be associated with complications, esp. bleeding: location of the polyp in the colon (right, left, rectum)
Factors associated with complications: polyp histology
Factors that may be associated with complications, esp. bleeding
Factors associated with complications: polyp morphology
Factors that may be associated with complications, esp. bleeding
Factors associated with complications: polyp resection time
Factors that may be associated with complications, esp. bleeding
Full Information
NCT ID
NCT05029934
First Posted
August 29, 2021
Last Updated
July 1, 2023
Sponsor
Universitätsklinikum Hamburg-Eppendorf
1. Study Identification
Unique Protocol Identification Number
NCT05029934
Brief Title
Efficacy of EndoClot™ Spraying After Endoscopic Resection of Large Colorectal Polyps
Acronym
EndoClot™
Official Title
Efficacy of EndoClot™ Spraying After Endoscopic Resection of Large Colorectal Polyps: A Randomized Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Terminated
Why Stopped
insufficient recruitment of study patients
Study Start Date
August 18, 2021 (Actual)
Primary Completion Date
January 27, 2023 (Actual)
Study Completion Date
January 27, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The effectiveness of colonoscopy in reducing colorectal cancer mortality relies on the detection and removal of neoplastic polyps. Effective and safe resection of larger polyps is particularly important due to their higher potential of malignancy. Large polyps ≥20mm are removed by so-called endoscopic mucosal resection (EMR) (and occasionally endoscopic submucosal dissection (ESD)) using electrocautery snares. Resection of these large polyps is associated with a risk of severe complications that may require hospitalization and additional interventions. The most common risk is delayed bleeding which is observed in approximately 2-10% of patients. In a recent randomized trial, clipping has been shown to reduce bleeding esp. on the right colonic side. However, clipping of larger areas is time consuming and may add to costs in several ways.
Our primary aim is to examine whether EndoClot™ application (a special form of longer lasting spray on the mucosal defect after EMR/ESD of large non-pedunculated colorectal polyps (≥20mm) will reduce the risk of delayed bleeding. We hypothesize that EndoClot™ application will reduce the risk of delayed bleeding by at least 3/4 (i.e. from 7.5% to 1.5%) based on an initial assumption of a 7.5% delayed bleeding rate.
Detailed Description
Colorectal cancer is the second most common cause of cancer death in the United States and Europe. The effectiveness of colonoscopy in reducing the risk of dying from colorectal cancer relies on the detection and safe resection of neoplastic polyps to prevent incident cancers. Most polyps are small and can be easily removed using snare with or without electrocautery. Because the risk of prevalent cancer or transition to cancer increases with polyp size, effective and safe resection of large polyps is particularly important.
Endoscopic mucosal resection (EMR) is evolving as the primary endoscopic technique to remove large non-pedunculated polyps. These flat or sessile polyps are defined as lateral spreading tumors with a low vertical axis that extend laterally along the luminal wall. Several mostly retrospective studies from Europe, the U.S. and Japan, have demonstrated a high "cure" rate, with results lending credence to the shift from surgical resection to endoscopic management of these lesions. Of concern, however, is 1) a fairly high overall complication rate of 8-26% in prospective studies3-7, and 2) as well the persistence of residual neoplasia on follow-up endoscopy ranging from 16% to 46%3, 6, 8. The former is the main topic of the present study.
Severe complications including bleeding associated with a standard diagnostic or screening colonoscopy, which may include resection of predominantly smaller polyps, are uncommon. Significant bleeding occurs in 0.2 to 0.5% of patients (defined as a 2mg drop in Hemoglobin) 9, 10. The risk of severe complications increases with polyp size; here, again, the most common complication is bleeding reported in 2 to 24% of polyp resections. In one recent analysis the rate of delayed bleeding in colonic EMR was 7.5%1.
In addition to size, other factors may affect complications. These include type of resection (piecemeal versus en-bloc), polyp location (right colon with a thinner wall than the left colon), age and comorbidities, especially those that affect clotting abilities (e.g. renal insufficiency, liver disease, use of anticoagulation). Studies that have examined variables, which may directly decrease the risk of complications associated with large polyp resection, are limited.
It is apparent that resection of a large polyp leaves behind a large mucosal defect. The mucosal ulcer that forms after polyp resection can take several weeks to heal. Bleeding complications typically occur within 7 to 10 days, requiring often admission, a repeat colonoscopy to stop bleeding, and possible blood transfusions. The rates depend on size, and have been shown to be around 1.5%-2.6% overall. It is significantly higher in larger adenomas of 2 cm and more, namely 6.5% in another recent meta analysis.
To reduce the risk of bleeding various measures have been proposed which also have been summarized in several recent meta analyses. These include coagulation, clipping and others, but only few randomized trials are available: Coagulation not effective in a recent meta analysis14, but only 4 of the 12 studies were randomized and these included all mostly smaller polyps or polyps of all sizes or pedunculated polyps. In a recent randomized trial, clipping has been shown to reduce bleeding esp. on the right colonic side. However, clipping of larger areas is time consuming and may add to costs in several ways.
Our primary aim is to examine whether EndoClot™ application (a special form of longer lasting spray on the mucosal defect after EMR/ESD of large non-pedunculated colorectal polyps (≥20mm) will reduce the risk of delayed bleeding. We hypothesize that EndoClot™ application will reduce the risk of delayed bleeding by at least 3/4 (i.e. from 7.5% to 1.5%) based on an initial assumption of a 7.5% delayed bleeding rate.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wound Endoscopical, Colon, After Polyp Resection, Colon
Keywords
colon endoscopic mucosa resection (EMR), delayed bleeding, colonoscopy, polyp resection
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
use of EndoClot adhesive after resection vs no use of any preventive action against delayed bleeding (control group)
Masking
Participant
Masking Description
Patients will not be informed about the use of EndoClot adhesive
Allocation
Randomized
Enrollment
96 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EndoClot group
Arm Type
Active Comparator
Arm Description
patients who are being provided with EndoClot adhesive spray after polyp resection
Arm Title
Control group
Arm Type
Sham Comparator
Arm Description
no further prophylactic bleeding prevention after polyp resection
Intervention Type
Procedure
Intervention Name(s)
use of EndoClot
Intervention Description
deployment of EndoClot adhesive spray
Primary Outcome Measure Information:
Title
delayed bleeding complication: hospitalization
Description
hospitalization after subsequent return to unit / health care facility for evaluation of rectal bleeding
Time Frame
30 days
Title
delayed bleeding complication: transfusion
Description
a patient who subsequently had to return to the unit and/or any health care facility for evaluation of rectal bleeding AND who required transfusion
Time Frame
30 days
Title
delayed bleeding complication: repeat endoscopy
Description
a patient who subsequently had to return to the unit and/or any health care facility for evaluation of rectal bleeding AND who required a repeat colonoscopy or sigmoidoscopy for examination of the polypectomy site or control of bleeding
Time Frame
30 days
Title
delayed bleeding complication:
Description
a patient who subsequently had to return to the unit and/or any health care facility for evaluation of rectal bleeding AND who required surgery
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Technical handling
Description
product deployment assumed quantity of entire vial: < 50%/50-70%/100%
Time Frame
20 minutes (assumed deployment time)
Title
Overall complications
Description
an aggregate of all complications that occur at the time of the procedure or during follow-up
Time Frame
procedure to day 30
Title
Factors associated with complications: polyp size
Description
Factors that may be associated with complications, esp. bleeding
Time Frame
30 days
Title
Factors associated with complications: polyp location
Description
Factors that may be associated with complications, esp. bleeding: location of the polyp in the colon (right, left, rectum)
Time Frame
30 days
Title
Factors associated with complications: polyp histology
Description
Factors that may be associated with complications, esp. bleeding
Time Frame
30 days
Title
Factors associated with complications: polyp morphology
Description
Factors that may be associated with complications, esp. bleeding
Time Frame
30 days
Title
Factors associated with complications: polyp resection time
Description
Factors that may be associated with complications, esp. bleeding
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with a ≥20mm colon non-pedunculated polyp who are undergoing an ESD or EMR resection
signed Informed Consent
Exclusion Criteria:
Patients with known (biopsy proven) or strongly suspected invasive carcinoma in a potential study polyp
Pedunculated polyps (as defined by Paris Classification type Ip or Isp)
ulcerated depressed lesions (as defined by Paris Classification type III)
polyposis syndromes
inflammatory bowel disease
emergency colonoscopy
Poor general health (ASA (American Society of Anaesthesiologists) class>3)
Patients with coagulopathy with an elevated International Normalized Ratio (INR )≥1.5, or platelets <50
Poor bowel preparation
pregnancy or breastfeeding
Intervention planned using ORISE™ (Boston Medical) or LIFTUP™ (Ovesco) as lifting agents
Facility Information:
Facility Name
Vivantes Auguste-Viktoria-Klinikum
City
Berlin
ZIP/Postal Code
12099
Country
Germany
Facility Name
University Hospital Hamburg Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
Facility Name
Evangelisches Amalie Sieveking Krankenhaus
City
Hamburg
ZIP/Postal Code
22359
Country
Germany
Facility Name
UKGM Marburg, Klinik für Gastroenterologie
City
Marburg
ZIP/Postal Code
35043
Country
Germany
Facility Name
Klinikum Südstadt Rostock
City
Rostock
ZIP/Postal Code
18059
Country
Germany
12. IPD Sharing Statement
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Efficacy of EndoClot™ Spraying After Endoscopic Resection of Large Colorectal Polyps
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