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Heat treatment after removing large colon polyps to prevent regrowth

Tests added heat treatment after removing large flat colon polyps, in adults.

Plain-language title generated from the registry record
Registry title: Reducing Neoplasia Recurrence After Non-thermal Endoscopic Resection of Large Colorectal Polyps

Key facts

Where
Montreal, CanadaSee the site

Where in Canada

  • Centre Hospitalier de l'Université de MontréalMontreal, CanadaNo longer taking part

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Trial details

Who runs it
Centre hospitalier de l'Université de Montréal (CHUM)
Trial code
NCT07242820
Record updated
14 August 2026
Original description
The goal of this clinical trial is to clarify the role of adjuvant thermal ablation for non-thermal endoscopic mucosal resection (EMR) of large (≥20mm) flat colorectal polyps (so-called laterally spreading lesions [LSLs]).Read full original descriptionShow less

Reducing Neoplasia Recurrence After Non-thermal Endoscopic Resection of Large Colorectal Polyps

The goal of this clinical trial is to clarify the role of adjuvant thermal ablation for non-thermal endoscopic mucosal resection (EMR) of large (≥20mm) flat colorectal polyps (so-called laterally spreading lesions [LSLs]).

The hypothesis is that adding adjuvant thermal ablation to non-thermal EMR (vs no ablation) will result in lower lesion recurrence rates at 6-month follow-up, and non-inferior adverse events (AE) rates 14 days post EMR.

For participants with planned EMR, endoscopists will perform non-thermal EMRs as per standard of care and:

* adjuvant thermal ablation will either not be performed (control group), or will be applied to the base and outside margins of the resection site (experimental group); * then, all patients will be contacted 14-44 days after EMR, to verbally ascertain the occurrence of AEs; * then, all patients will undergo a first follow-up colonoscopy at 6 months after initial conoloscopy to assess lesion recurrence; * finally, all patients will undergo a second and final colonoscopy 18 months after EMR.

Inclusion: Adult patients; Undergoing EMR for large (≥20 mm) colorectal LSL; Providing written and informed consent for study participation.

Exclusion: Inflammatory bowel disease; Coagulopathy or thrombocytopenia (international normalized ration ≥1.5 or platelets <50*10\^9/L); Non-elective colonoscopy; Poor general health (American Society of Anesthesiologists classification >III); Bulky lesions (granular mixed with ≥10mm module).

ClinicalTrials.gov NCT07242820