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EMR Versus ESD for Resection of Large Distal Non-pedunculated Colorectal Adenomas

Multicenter, Randomised Controlled Trial Comparing Endoscopic Mucosal Resection (EMR) And Endoscopic Submucosal dissecTIon (ESD) for Resection of Large Distal Non-pedunculated Colorectal Adenomas (MATILDA-trial)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02657044
Acronym
MATILDA
Enrollment
212
Registered
2016-01-15
Start date
2016-04-30
Completion date
2020-12-31
Last updated
2016-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms

Keywords

EMR, ESD, endoscopic mucosal resection, endoscopic submucosal resection, colorectal adenomas

Brief summary

Endoscopic resection of adenomas in the colon is the cornerstone of effective colorectal cancer prevention. Endoscopic mucosal resection (EMR) is currently the most used technique for resection of large distal colorectal adenomas, however, maintains some important limitations. In large lesions, EMR can often only be performed in a piecemeal fashion resulting in relatively low R0-resection rates and high recurrence rates. Endoscopic submucosal dissection (ESD) is a newer procedure that is more difficult resulting in a longer procedural time, but is promising due to the high en-bloc resection rates and the very low recurrence rates. The aim of this multicenter randomized study is to compare EMR and ESD with regard to recurrence rates and radical (R0) resection rates, and to put this into perspective against the costs and complication rates of both strategies and the burden perceived by patients on the long term-term.

Interventions

PROCEDUREEMR
PROCEDUREESD

Sponsors

Comprehensive Cancer Centre The Netherlands
CollaboratorOTHER
UMC Utrecht
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* non-pedunculated polyp larger than 20 mm in the rectum, sigmoid or descending colon found during colonoscopy * indication for endoscopic treatment * ≥18 years old * Written informed consent

Exclusion criteria

* suspicion of malignancy, as determined by endoscopic findings (invasive Kudo pit pattern, Hiroshima type C) or proven malignancy at histology * prior endoscopic resection attempt * presence of synchronous distal advanced carcinoma that requires surgical resection * the risk exceeds the benefit of endoscopic treatment, such as patient's with an extremely poor general condition or a very short life expectancy * the inability to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Recurrence rate at follow-up colonoscopy after 6 months6 monthsObserved from resected residual disease or, if not present, from biopsies of the scar

Secondary

MeasureTime frameDescription
R0-resection rate30 daysDefined as dysplasia free vertical and lateral resection margins at histology
Long-term recurrence rate at follow-up colonoscopy after 36 months36 monthsObserved from resected residual disease or, if not present, from biopsies of the scar
Surgical referral rate36 monthsDefined as the number of patients that are referred for surgical management at 36 months
Perceived burden and quality of life among patients36 monthsMeasurement of the patients' burden of ESD versus EMR will be evaluated with regard to colorectal cancer anxiety, burden of the procedure itself, functional complaints and overall quality of life. Meaurement will be performed using validated questionnaires.
Complication rate30 daysComplications will be assessed on day 30: intraprocedural perforation, Intraprocedural bleeding, Postprocedural bleeding, Postprocedural perforation, Postprocedural serositis.
Health care resource utilization and consts36 monthsHealthcare costs will be calculated by multiplying used healthcare services with unit prices. The cost-effectiveness of ESD against EMR will be expressed as incremental cost-effectiveness ratios (ICER) showing additional costs per recurrence free patient and as ICER showing additional costs per QALY.

Countries

Netherlands

Contacts

Primary ContactY. Backes, MD
y.backes@umcutrecht.nl003187550722

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026