AzTrials
AzTrials

Colonic AdenomaPROSPERNCT02957058

PROSpective Assessment of Post EmR Recurrence

A study testing SCAR technique in people with Colonic Adenoma and Colonic Polyp, run by Western Sydney Local Health District at 1 site in Australia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

To prospectively validate the SERT (Sydney EMR Recurrence Tool) scoring system for adenoma recurrence rates around the endoscopic mucosal resection (EMR) scar after wide field-EMR with thermal treatment applied to the defect margin. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Colonic Adenoma, Colonic Polyp
What is being tested?
SCAR technique
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
700 participants
Where
1 siteAustralia
Study dates
Jan 2017to Apr 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • All laterally spreading lesions >= 20mm referred to the named tertiary referral centres
  • Must consent to involvement

Who cannot join

  • Histology other than specified
  • Lesion involving the ileocaecal valve
  • Pregnancy: currently pregnant or attempting to become pregnant
  • Lactation: currently breastfeeding
  • Taken clopidogrel within 7 days
  • Taken warfarin within 5 days
Show all 10Show fewer
  • Had full therapeutic dose unfractionated heparin within 6 hours
  • Had full therapeutic dose low molecular weight heparin (LMWH) within 12 hours
  • Known clotting disorder
  • Previous attempt at EMR of the polyp referred for resection

Trial locations and contacts

1 site in 1 country.

Australia1 site
  • Westmead Hospital

    Westmead, New South Wales, 2145

Other trials in Australia

About this study

Official title: A Prospective Study Stratifying Patients to Follow up Intervals Based on Risk of Recurrence Post Wide Field Colonic EMR

To prospectively validate the SERT (Sydney EMR Recurrence Tool) scoring system for adenoma recurrence rates around the endoscopic mucosal resection (EMR) scar after wide field-EMR with thermal treatment applied to the defect margin. The primary aim of the study will be to ensure the safety of this approach and there will be constant monitoring to ensure that this is the case.

Read the detailed description

Colonoscopy and polypectomy reduces the anticipated incidence of colorectal malignancy in patients with significant adenomatous polyps by approximately 80% in long term follow up. Most endoscopists routinely perform removal of small polyps. However, removal of flat colonic neoplasia 20mm in size or larger is more complex and requires specific endoscopic techniques, one such technique being termed wide field endoscopic mucosal resection (WF-EMR). Traditionally these lesions were treated surgically at significant expense to the healthcare system. Endoscopic treatment of large colonic polyps reduces health care costs by approximately $11,000 per patient treated, saves bed days and avoids surgery in more than 90% of patients.

EMR describes the endoscopic technique of treating colorectal adenomatous polyps with submucosal lifting and careful piecemeal snare resection. This procedure has been shown to be safe and effective at resecting lesions limited to the mucosa. Clearly the importance of predicting lesions that are unlikely to have invaded the deeper layers is of the utmost importance here, and significant improvements in our ability to assess this have been made in large volume centres such as Westmead

An important longer-term complication of EMR of large flat colonic neoplasia is the phenomenon of residual polyp tissue or polyp recurrence, which will be the focus of the proposed research study. Recurrence is detected by surveillance colonoscopies (SC), which are performed at defined intervals after the index procedure. Our current standard for safe surveillance interval at Westmead after >= 20mm EMR is 5 months (SC1). In the largest study to date, the Australian Colonic EMR (ACE) study, recurrence at SC1 stands at 16.5% for all patients.

We have recently come to the end of a randomised trial (SCAR) of thermal treatment (snare tip soft coagulation, STSC) of the EMR defect margin (SCAR technique), with the findings to be presented at the Digestive Diseases Week in San Diego. The results of this trial (n=353) are promising with a risk of adenoma recurrence in the treated group of 6.4% vs 20.7% in the non-treated group (relative risk 0.3, p < .001). There have been no adverse events related to this treatment. The investigators plan to perform this intervention on all patients in the proposed study.

In addition, there is increasing evidence, both in the scientific literature and at our institution, that there are identifiable factors at the initial EMR that predict recurrence at SC1. Current data from the ACE cohort suggests that increasing size of lesion (>=40mm), presence of high grade dysplasia (HGD) in the resection specimen and intra-procedural bleeding requiring endoscopic control predict greater likelihood of recurrence. The investigators have created, and have submitted for publication, a risk score for recurrence after EMR known as the Sydney EMR Recurrence Tool (SERT), (figure 1). SERT was created by binomial logistic regression analysis (figure 2) on 692 patients (model cohort) from the ACE study and validated on the remaining 691 patients (validation cohort) who had undergone SC1. Kaplan Meier curves (figure 3) were used to determine the predicted incidence of recurrence at various points in time after EMR on the validation cohort (figure 4). The strength of SERT lies in predicting the absence of recurrence, with negative predictive value of 92.6% at first surveillance colonoscopy. While this score was not derived from patients treated with SCAR technique, it is expected that the stratification of lesions by SERT will continue to be valid with lower overall rates.

Crucial in ensuring the absence of polyp recurrence in the long term is surveillance colonoscopy. In the endoscopy department at Westmead the current standard of follow-up is SC1 at 5 months. This short interval is costly and inconvenient for patients, but has been thought necessary due to previous anxiety over recurrence rates.

The investigators therefore propose a study to prospectively evaluate recurrence after WF-EMR by triaging follow up based on SERT, with all lesions treated by SCAR technique. Patients with SERT 0 lesions would be triaged to first follow up at 18 months (the usual time for SC2) since their rate of recurrence until this point is predicted to be very low (8.5%) and such recurrence is likely to be easily treated endoscopically after this time (in the validation cohort recurrence was commonly diminutive (<5mm, 67%), uni-focal (75%), with no high grade dysplasia (HGD). All recurrences were treatable endoscopically. This compares favourably to the 90.3% successful endoscopic treatment of recurrence rate in a recent meta-analysis.

Higher risk lesions (SERT 1-4) would be triaged to earlier follow up at 6 then 18 months, since their predicted risk of recurrence at 6 months is 14.8% and at 18 months is 31.8%. All lesions would require a follow up procedure at approximately 36 months after the original EMR since both groups rate of recurrence increases by this time (figure 4) and this will be suggested to the referring specialist.

Risk factor Score Laterally Spreading lesion Size >= 40, score 2 Intraprocedural bleeding requiring endoscopic control, score 1 High grade dysplasia, score 1

Being tested
SCAR technique
Keywords
Colonoscopy, Endoscopic Mucosal Resection, Adenoma Recurrence, EMR defect thermal ablation
Medical subject headings
Colonic Polyps

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • SCAR techniqueProcedure or surgery

    Thermal ablation of the EMR margin using ERBE Soft Coagulation (Effect 4, 80 watts) and the operator choice of endoscopic resection snare

Study groups in NCT02957058
Study groupRoleWhat they receive
SERT 0, SCAR (low risk)Active comparatorPatients with Sydney EMR Recurrence Tool (SERT scoring) score 0. These patients will be invited to return for follow up at 18 months and will have thermal ablation (SCAR technique) of the endoscopic resection defect margin.
Receives: Procedure: SCAR technique
SERT 1-4, SCAR (high risk)Active comparatorPatients with Sydney EMR Recurrence Tool score 1-4 (SERT scoring). These patients will be invited to return for follow up at 4-6 months and will have thermal ablation (SCAR technique) of the endoscopic resection defect margin.
Receives: Procedure: SCAR technique

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Adenoma recurrence

    Recurrence of adenoma at first and second surveillance colonoscopy

    Measured: Variable dependent on SERT score

Secondary outcomes (4)
  1. Need for surgery

    need for surgery due to adenoma recurrence or complication

    Measured: 18 months

  2. Bleeding after EMR

    Measured: 2 weeks

  3. Pain after EMR

    Measured: 2 weeks

  4. Delayed perforation after EMR

    Measured: 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Nov 2016 (estimated)
  2. Study startJan 2017
  3. Primary completionJan 2022
  4. Study completionApr 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
700 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02957058
Sponsor's protocol ID
AU RED HREC/16/WMEAD/130
Acronym
PROSPER
Status last verified
Mar 2025
First submitted
3 Nov 2016
Last updated
27 Mar 2025
Results posted
No
Data monitoring committee
Yes

Publications

  • Sidhu M, Shahidi N, Gupta S, Desomer L, Vosko S, Arnout van Hattem W, Hourigan LF, Lee EYT, Moss A, Raftopoulos S, Heitman SJ, Williams SJ, Zanati S, Tate DJ, Burgess N, Bourke MJ. Outcomes of Thermal Ablation of the Mucosal Defect Margin After Endoscopic Mucosal Resection: A Prospective, International, Multicenter Trial of 1000 Large Nonpedunculated Colorectal Polyps. Gastroenterology. 2021 Jul;161(1):163-170.e3. doi: 10.1053/j.gastro.2021.03.044. Epub 2021 Mar 31.

    PubMed 33798525

Questions about this trial

What is this clinical trial studying?

A study testing SCAR technique in people with Colonic Adenoma and Colonic Polyp, run by Western Sydney Local Health District at 1 site in Australia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Australia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Adenoma recurrence (time frame: Variable dependent on SERT score). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02957058, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Mar 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in