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Clip Placement Following Colonic Endoscopic Mucosal Resection (EMR) (CLIPPER)

Primary Purpose

Polyp, Colonic, Bleeding

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Olympus Quick Clip Pro - Single Use Repositionable Clips
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Polyp, Colonic

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • laterally spreading or sessile polyp morphology (Paris classification 0-IIa/b/c) proximal to the splenic flexure, measuring 2-6 cm
  • All patients aged >18 years undergoing an EMR
  • Written informed consent

Exclusion Criteria:

  • Previous resection or attempted resection of a lesion less than 30 days ago or in the same session,
  • Clip deployed prior to the completion of the EMR for a perforation or a major intra-procedural bleeding not treatable by coagulation,
  • Endoscopic appearance of invasive malignancy (non-lifting Kato D, Kudo V pit pattern),
  • Pregnancy,
  • Active inflammatory colonic conditions (e.g. inflammatory bowel disease),
  • Insufficiently corrected anticoagulants AND/OR a clotting disorder (platelet count <50x109/l, INR > 1,5),
  • American Society of Anesthesiology (ASA) Grade IV-V,
  • Macroscopic non-radical resection,
  • >1 lesion in 1 session,
  • Involvement of valvula Bauhin or appendiceal orificium

Sites / Locations

  • Ziekenhuis St Jansdal
  • Radboudumc

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Clip group

Control group

Arm Description

Olympus Quick Clip Pro - Single Use Repositionable Clips will be used for Prophylactic clipping after EMR

Standard treatment after EMR (as described in the detailed study description above)

Outcomes

Primary Outcome Measures

Delayed bleeding
Clinical relevant delayed bleeding defined according to the ASGE working party document for adverse events in coloscopy.

Secondary Outcome Measures

Adenoma recurrence
Recurrence rate will be determined by endoscopy and biopsies.
Cost-effectiveness
A cost effectiveness analysis will be done, based on length of hospital stay and professional medical attendance and aided by an estimation of the impact on quality of health by the questionnaires EQ-5D, iMCQ, iPCQ.
EMR scar evaluation
EMR scars will be evaluated by endoscopic photography and biopsies.

Full Information

First Posted
October 9, 2017
Last Updated
March 29, 2023
Sponsor
Radboud University Medical Center
Collaborators
UMC Utrecht, Maastricht University Medical Center, Erasmus Medical Center, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), Maxima Medical Center, Jeroen Bosch Ziekenhuis, Bernhoven Hospital, Isala, Canisius-Wilhelmina Hospital, Maasstad Hospital, Noordwest Ziekenhuisgroep, Meander Medisch Centrum, Catharina Ziekenhuis Eindhoven, Elisabeth-TweeSteden Ziekenhuis, St Jansdal Hospital, Leiden University Medical Center, Dutch Digestive Diseases Foundation, Franciscus Gasthuis, Bravis Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03309683
Brief Title
Clip Placement Following Colonic Endoscopic Mucosal Resection (EMR)
Acronym
CLIPPER
Official Title
Clip Placement Following Colonic Endoscopic Mucosal Resection (EMR). The CLIPPER Study: A Nationwide Multi-center Randomized Clinical Trail
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
March 5, 2018 (Actual)
Primary Completion Date
August 19, 2022 (Actual)
Study Completion Date
March 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
UMC Utrecht, Maastricht University Medical Center, Erasmus Medical Center, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), Maxima Medical Center, Jeroen Bosch Ziekenhuis, Bernhoven Hospital, Isala, Canisius-Wilhelmina Hospital, Maasstad Hospital, Noordwest Ziekenhuisgroep, Meander Medisch Centrum, Catharina Ziekenhuis Eindhoven, Elisabeth-TweeSteden Ziekenhuis, St Jansdal Hospital, Leiden University Medical Center, Dutch Digestive Diseases Foundation, Franciscus Gasthuis, Bravis Hospital

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
Study design: A national, multi-center, patient-blinded, randomized clinical trial. Study population: Patients undergoing EMR with a moderate to severe risk (right sided colon, ≥2cm) of developing Delayed Bleeding (DB). Intervention: PC will be compared to standard care (no PC). Main study endpoints: Primary endpoint is the incidence of DB. Secondary endpoints are cost-effectiveness, quality of life and (severe) adverse events related to PC, adenoma recurrence and risk factors for DB.
Detailed Description
Design This is a multi-center, randomized, patient-blinded multicenter trial, comparing two treatment strategies in 356 patients undergoing EMR for a colonic lesion 2-6 cm. The study will be enrolled in a selection of academic and non-academic Dutch hospitals. Patients undergoing an EMR will be a randomly allocated by web-based randomization to: A) PC treatment group: minimally 1 clip per 1 cm of the polyp resection plane: OR B) Control group: standard care: only clip placement in case of uncontrollable bleeding (not successfully managed by coagulation) AND/OR perforation. Population The target population in this proposal includes patients of 18 years and older, who gave written informed consent, undergoing EMR of a colonic polyp with a moderate to severe risk of developing DB. Moderate-severe risk of DB is defined as a laterally spreading or sessile polyp morphology proximal to the splenic flexure, measuring 2-6cm. Given the significantly increased risk of bleeding in the cecum, ascending and transverse colon, clip placement at this location may have the greatest benefit. Inclusion Gastroenterologists from participating hospitals of the Dutch EMR Study Group will be asked to recruit patients for the trial. They will provide written information about the trial to potential participants, i.e., all patients scheduled for an EMR of a (right-sided) colonic polyp 2-6 cm, and 18 years or older. Members of the study group will contact potentially eligible patients at the outpatient clinic, hospital wards or by phone and give detailed information about the trial. In- and exclusion criteria will be checked and questions about the trial will be answered. Eligible patients will be invited to participate. After both the patient and the study physician or nurse practitioner have signed the informed consent form, in- and exclusion criteria will be checked again and baseline measurements will be performed, which include disease specific questionnaires including risk-factors for DB (AC use, restarting AC, polyp size, visible vessel, etc) and generic and disease specific quality of life questionnaires (see below). Patient's contact details will be provided to the study center for randomization. Standard of care (usual care) In Dutch common practice, PC is not standard of care. PC is used, based on the personal preference of the endoscopist, mostly in case of intra-procedural bleeding/(possible)perforation. In our study group the minority of endoscopists applies PC after EMR in case of high risk patients, defined as right-sided flat polyps of at least 2cm and on AC or AP therapy. Definition clinical significant delayed bleeding (DB) DB is defined as any bleeding occurring after the completion of the procedure necessitating blood transfusion, hospitalization, or re-intervention (either repeat endoscopy, angiography, or surgery). Self-limiting bleeding managed on an outpatient basis is not included. Severity of DB Severity of bleeding is defined according to the ASGE working party document for adverse events in colonoscopy: Mild DB: any post-EMR medical consultation, unplanned hospital admission, or prolongation of hospital stays for 3 days or fewer. Moderate DB: unplanned hospital admission of 4 to 10 days, transfusion, repeat endoscopy, any interventional radiology procedure, or intensive care unit (ICU) admission for 1 night. Severe DB: admission to the ICU for more than 1 night, unplanned admission for more than 10 nights, surgery, or permanent disability. Treatment of DB DB is primarily treated by resuscitation. In case of resuscitation failure, colonoscopy, angiography with coiling and eventually surgery may be applied to control the bleeding site. Follow-up After the EMR patients are contacted at 30, 90 and 180 days (short-term and long-term effects). At 180 days a colonoscopy is scheduled to access the adenoma recurrence rate (standard of care).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polyp, Colonic, Bleeding

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
356 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Clip group
Arm Type
Experimental
Arm Description
Olympus Quick Clip Pro - Single Use Repositionable Clips will be used for Prophylactic clipping after EMR
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Standard treatment after EMR (as described in the detailed study description above)
Intervention Type
Device
Intervention Name(s)
Olympus Quick Clip Pro - Single Use Repositionable Clips
Other Intervention Name(s)
prophylactic clipping, hemoclip
Intervention Description
A hemoclip will be placed after every 0,5-1,0 cm of the resected area to proximate wound edges.
Primary Outcome Measure Information:
Title
Delayed bleeding
Description
Clinical relevant delayed bleeding defined according to the ASGE working party document for adverse events in coloscopy.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Adenoma recurrence
Description
Recurrence rate will be determined by endoscopy and biopsies.
Time Frame
180 days
Title
Cost-effectiveness
Description
A cost effectiveness analysis will be done, based on length of hospital stay and professional medical attendance and aided by an estimation of the impact on quality of health by the questionnaires EQ-5D, iMCQ, iPCQ.
Time Frame
180 days
Title
EMR scar evaluation
Description
EMR scars will be evaluated by endoscopic photography and biopsies.
Time Frame
180 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: laterally spreading or sessile polyp morphology (Paris classification 0-IIa/b/c) proximal to the splenic flexure, measuring 2-6 cm All patients aged >18 years undergoing an EMR Written informed consent Exclusion Criteria: Previous resection or attempted resection of a lesion less than 30 days ago or in the same session, Clip deployed prior to the completion of the EMR for a perforation or a major intra-procedural bleeding not treatable by coagulation, Endoscopic appearance of invasive malignancy (non-lifting Kato D, Kudo V pit pattern), Pregnancy, Active inflammatory colonic conditions (e.g. inflammatory bowel disease), Insufficiently corrected anticoagulants AND/OR a clotting disorder (platelet count <50x109/l, INR > 1,5), American Society of Anesthesiology (ASA) Grade IV-V, Macroscopic non-radical resection, >1 lesion in 1 session, Involvement of valvula Bauhin or appendiceal orificium
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erwin JM Van Geenen, dr
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ziekenhuis St Jansdal
City
Harderwijk
State/Province
Gelderland
ZIP/Postal Code
3844DG
Country
Netherlands
Facility Name
Radboudumc
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525GA
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Open for sharing IPD after study completion and publication. Currently not yet applicable as the study is still recruiting.
Citations:
PubMed Identifier
33461579
Citation
Turan AS, Moons LMG, Schreuder RM, Schoon EJ, Terhaar Sive Droste JS, Schrauwen RWM, Straathof JW, Bastiaansen BAJ, Schwartz MP, Hazen WL, Alkhalaf A, Allajar D, Hadithi M, van der Spek BW, Heine DGDN, Tan ACITL, de Graaf W, Boonstra JJ, Voogd FJ, Roomer R, de Ridder RJJ, Kievit W, Siersema PD, Didden P, van Geenen EJM; Dutch EMR Study Group. Clip placement to prevent delayed bleeding after colonic endoscopic mucosal resection (CLIPPER): study protocol for a randomized controlled trial. Trials. 2021 Jan 18;22(1):63. doi: 10.1186/s13063-020-04996-7.
Results Reference
derived

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Clip Placement Following Colonic Endoscopic Mucosal Resection (EMR)

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