ACER/AMN: The Australian Colonic Advanced Mucosal Neoplasia and Endoscopic Resection Study

Sponsor
Professor Michael Bourke (Other)
Overall Status
Recruiting
CT.gov ID
NCT02000141
Collaborator
(none)
2,000
1
240
8.3

Study Details

Study Description

Brief Summary

To enhance understanding of the risk factors for AMN, improve lesion assessment and prediction of submucosal invasive cancer, improve endoscopic resection efficacy, reduce complications of WF-EMR and improve the understanding of the progression of large lesions to cancer

Condition or Disease Intervention/Treatment Phase
  • Procedure: Endoscopic Mucosal Resection

Detailed Description

The Australian Colonic Endoscopic Mucosal Resection study (ACE), is a multicentre prospective observational study which examined WF-EMR of colonic AMN (Ethics approval No. HREC JH/TG 2008/9/6.1(2858)). This project now has an extensive dataset from 8 leading colonic endoscopic resection centres in Australia on more than 1500 lesions resected over 4 years since June 2008.

The ACE study has been successful in addressing several aspects of the resection of AMN, resulting in several high profile papers in internationally recognised journals. The collection of this data has produced robust information on the efficacy of the procedure4, recurrence rates7, bleeding complications8 and mortality when compared to surgery5. Single centre analysis of the ACE dataset at Westmead has also allowed insights into how to refine the procedure to improve outcomes. The target sign is now a recognised indication for the placement of clips to prevent perforation9, CO2 insufflation for WF-EMR has been shown to be superior to air insufflation10 and succinylated gelatin (Gelofusine®) has been shown to be superior to normal saline as a submucosal lifting agent11.

There remain a number of unanswered questions regarding the endoscopic resection of large sessile lesions and expanding the ACE dataset in a new cohort of patients will allow these to be addressed. Enhancing the prediction of submucosal invasive cancer, advanced lesion classification, refinement of the assessment of deep injury, submucosal injectate constituents, the optimum electrosurgical resection methods, prevention and prophylaxis of bleeding, and subtype analyses of the different histological groups comprising AMN will be examined.

Study Design

Study Type:
Observational
Anticipated Enrollment :
2000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Australian Colonic Advanced Mucosal Neoplasia and Endoscopic Resection Study - a Prospective Observational Cohort Study
Study Start Date :
Jan 1, 2014
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Jan 1, 2034

Arms and Interventions

Arm Intervention/Treatment
Endoscopic Mucosal Resection

Endoscopic Mucosal Resection of Colonic Advanced Mucosal Lesions

Procedure: Endoscopic Mucosal Resection

Outcome Measures

Primary Outcome Measures

  1. Recurrence [6-60 months]

    Follow up colonoscopies as per standard of care for 6 - 60 months noting and treating any recurrence.

Secondary Outcome Measures

  1. Cancer prediction [Initial procedure]

    By properly assessing the lesion it is hoped that we will be able to provide the greater Gastroenterology community with a tool which can be used to properly identify benign and cancerous lesions to decrease the number of benign lesions being referred to surgery.

  2. Improved Endoscopic Resection [0-60 months]

    By assessing the lesion at resection and following up with standard of care colonoscopies it is anticipated that there will be an improved endoscopic resection efficacy therefore reducing the risk of recurrence.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients referred for endoscopic resection of a large sessile colonic polyp or laterally spreading tumour ≥20mm in size.

  • Age > 18 years

  • Able to give informed consent to involvement in the clinical study

Exclusion Criteria:

• Unable to provide informed consent for involvement

Contacts and Locations

Locations

Site City State Country Postal Code
1 Westmead Endoscopy Unit Westmead New South Wales Australia 2145

Sponsors and Collaborators

  • Professor Michael Bourke

Investigators

  • Principal Investigator: Michael Bourke, MBBS, South West Sydney Area Health Service

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Professor Michael Bourke, Director of Gastrointestinal Endoscopy, Western Sydney Local Health District
ClinicalTrials.gov Identifier:
NCT02000141
Other Study ID Numbers:
  • HREC2013/8/4.5(3778)
  • AU RED HREC/13/WMEAD/233
First Posted:
Dec 3, 2013
Last Update Posted:
Mar 23, 2021
Last Verified:
Mar 1, 2021
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 23, 2021