FLOAT: DeFect cLOsure After Colonic ESD With underwaTer Technique

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Recruiting
CT.gov ID
NCT04214678
Collaborator
(none)
64
1
2
35.9
1.8

Study Details

Study Description

Brief Summary

This is a single centre randomised controlled study comparing underwater clip closure versus conventional gas insufflation clip closure of post-resection defect in patients undergoing colonic endoscopic resection. The investigators hypothesize that underwater clip closure would be faster than conventional closure under gas insufflation.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Underwater clip closure
  • Procedure: Conventional clip closure
N/A

Detailed Description

Endoscopic submucosal dissection (ESD) is a minimally invasive technique that has been increasingly applied to superficial colorectal tumours over the past two decades (1, 2). Although serious complications with this procedure are uncommon, both significant delayed haemorrhage (1-2%) and perforation (4-6%) are recognised complications (3). Although perforation is generally recognised and treated at time of endoscopy, delayed bleeding often requires repeat readmission and endoscopy for haemorrhage control. There is growing evidence to support prophylactic clip closure of mucosal defects to reduce incidences of delayed haemorrhage.

Prophylactic clip closure of mucosal defects (≥20mm) after colonic ESD is supported by large retrospective case series. In a series of 524 lesions in 463 patients, Liaquat et al. (2013) reported prophylactic clipping of resection sites to close mucosal defects versus non-closure, reduced delayed haemorrhage (9.7% vs 1.8%) (4). Ogiyama et al. (2018) reported similar findings in a series of 156 lesions (0% vs 8.2%, p=0.008) (5).

Prophylactic defect closure also has a theoretical benefit in reducing delayed perforation from unrecognised muscular breach during dissection. Though it is recognised that there is a paucity of evidence to support mucosal apposition in reducing delayed perforation rates (~0.2%) (3). This is likely due to the underpowered published studies and a very low event rate.

For these reasons, it has been routine practice of many endoscopists for clip closure of mucosal defects after endoscopic resection of large colorectal neoplasia. However, this technique remains technically challenging within the narrow colonic space and at times may not be feasible. The 'underwater closure technique' in mucosal defect closure of colonic and duodenal endoscopic resections has promising early results. Compared to conventional CO2 insufflation clip placement, at the time of mucosal closure this technique applies luminal water infusion to 'float' the resection borders and downsize the target. Early experience suggests this technique facilitates easier apposition of resection borders and complete closure. There are currently no randomized trials comparing these clip closure techniques.

The aim of the study is to evaluate whether prophylactic underwater closure technique facilitates easier ESD mucosal defect closure compared to conventional clip closure.

This is a single centre prospective randomized controlled trial. Consecutive patients undergoing endoscopic resection for colonic lesions would be recruited. Participants would be randomized to receive prophylactic conventional clip closure versus underwater technique.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
DeFect cLOsure After Colonic ESD With underwaTer Technique Versus Conventional Clip : a Randomized Controlled Trial
Actual Study Start Date :
Jul 1, 2020
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Underwater clip closure

The post-resection defect is closed using endoscopic clips with underwater technique

Procedure: Underwater clip closure
Closure of post-resection defect with endoscopic clips by underwater technique

Active Comparator: Conventional clip closure

The post-resection defect is closed using endoscopic clips with conventional gas insufflation (CO2)

Procedure: Conventional clip closure
Closure of post-resection defect with endoscopic clip by conventional technique

Outcome Measures

Primary Outcome Measures

  1. Time required to complete clip closure of mucosal defect [Within 1 hour]

    o Defined as the time from completion of prophylactic coagulation till the final clip application (min)

Secondary Outcome Measures

  1. Technical success of complete closure of defect (%) [Within 1 hour]

  2. Total time for endoscopic procedure (min) [Within 1 hour]

  3. Number of endoscopic clip used for closure [Within 1 hour]

  4. Rate of Haemorrhage [30 days]

    Post-procedural per rectal bleeding that requires intervention or blood product transfusion

  5. Rate of Perforation [30 days]

    Abdominal pain with radiological evidence of intra-abdominal free gas suggesting perforation

  6. Rate of Post-polypectomy electrocoagulation syndrome [30 days]

    Abdominal pain without radiological evidence of intra-abdominal free gas to suggest perforation

  7. Rate of Any other adverse event related to the procedure [30 days]

    Other adverse event

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients undergoing elective endoscopic resection

  • Colorectal superficial neoplasm with a resultant mucosal defect of ≥20mm

  • Age >18 years old

Exclusion Criteria:
  • Patients on anticoagulation (Warfarin or other direct oral anticoagulants)

  • Muscular perforation during the endoscopic resection

  • Incomplete endoscopic resection

  • Lesions arising from surgical anastomotic site

  • Marked electrolyte abnormalities

  • Other cases deemed by the examining physician as unsuitable for safe treatment

  • Patients who refused to participate

Contacts and Locations

Locations

Site City State Country Postal Code
1 Prince of Wales Hospital Hong Kong Hong Kong

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

  • Principal Investigator: Hon Chi Yip, MBChB, Chinese University of Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hon Chi Yip, Associate Consultant, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT04214678
Other Study ID Numbers:
  • CRE 2019.558
First Posted:
Jan 2, 2020
Last Update Posted:
Aug 16, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hon Chi Yip, Associate Consultant, Chinese University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 16, 2022