Skip to content

Endoscopic Full Thickness Resection Versus Standard Therapy of the Colorectal Neoplasia

Endoscopic Full Thickness Resection Versus Standard Therapy of the Colorectal Neoplasia - Prospective Randomized Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03868605
Enrollment
80
Registered
2019-03-11
Start date
2019-05-31
Completion date
2022-12-31
Last updated
2022-04-20

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

Conditions

Colon Cancer, Polyps

Brief summary

Most of the cancers develop from the adenomatous polyps. The therapeutic methods have been established already - endoscopic polypectomy (EPE) for stalked polyps and endoscopic mucosal resection (EMR) or endoscopic submucosal dissection (ESD) for non-pedunculated polyps. EMR is preferred in European countries over ESD because of its higher feasibility. However, the local residual neoplasia (LRN) after EMR has been reported in 14 - 24 % cases. There is a higher LRN risk in sessile polyps which do not elevate sufficiently after the submucosal injection (non-lifting sign) and the piece-meal resection needs to be used. Therefore, the new method of endoscopic full-thickness resection (FTR) has been developed to resect these lesions.

Detailed description

In this project, 80 individuals (age ≥ 18 years) with colorectal lesions of 10-25 mm size with positive non-lifting sign will be included. Such lesions might be found during the colonoscopies at the trial endoscopy centers or at the cooperating referring endoscopy centers outside the study. Patient will be scheduled for the index therapeutic colonoscopy (iTC) and randomized in two groups - FTR group (therapy with FTRD) and ST group (standard therapy, EMR or ESD due to the indication, decided by the endoscopist). First follow-up colonoscopy (FC1) will be performed in 6 months interval. In case of LRN negativity at FC1, the second follow-up colonoscopy (FC2) will be done after 12 months (18 months since iTC). In case of LRN positivity at FC1, the LRN therapeutic colonoscopy (LRN-TC) will follow with the endoscopic method due the findings (patients will be divided into four groups): APC group (LRN ≤ 5 mm; APC therapy), EMR group (LRN \> 5 mm and negative non-lifting sign negative; EMR therapy), FTR group (LRN \> 5 mm and positive non-lifting sign; therapy with FTRD) and surgery group (complex lesion; surgical therapy). In some LRN positive cases, FC1 will be the same as LRN-TC. The first follow-up colonoscopy after LRN therapy (LRN-FC1) will be performed after 6 months (12 months since TC). In case of re-LRN negativity at LRN-FC1 the second follow-up colonoscopy after LRN therapy (LRN-FC2) will be done after 6 months (18 months since iTC). In case of re-LRN positivity at LRN- FC1 the therapy will be done same as during FC1 and next follow-up will be done outside this trial. In some re-LRN positive cases, LRN-FC1 will be the same as re-LRN-TC. In conclusion, all patients will be followed-up within the study for 18 months, if timely possible.

Interventions

DEVICEEMR and ESD

Endoscopic mucosal resection using a resection snare Endoscopic submucosal dissection using an electrosurgical knife

DEVICEOver- the- scope full- thickness resection device

Endoscopic resection of neoplastic lesions of the colon using the over- the- scope full- thickness resection device

Sponsors

Masaryk University
CollaboratorOTHER
University Hospital Olomouc
CollaboratorOTHER
Military University Hospital, Prague
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

* age ≥ 18 years * colorectal lesions of 10-25 mm size with positive non-lifting sign * signed informed consent with the study and with colonoscopy

Exclusion criteria

* age \< 18 years * lesions \> 25 mm * pedunculated polyps * colorectal stenosis * colonoscopy contraindication * severe acute inflammatory bowel disease * severe comorbidities * patient not able to sign the informed consent

Design outcomes

Primary

MeasureTime frameDescription
Proportion of R0 procedures3 monthsproportion of patients with resection specimens with negative horizontal and vertical margins confirmed by histopathology

Secondary

MeasureTime frameDescription
Proportion of curative resections12 monthsProportion of the LRN at 6 months and 12 months follow-up colonoscopy after the index therapeutic colonoscopy

Countries

Czechia

Contacts

Primary ContactStepan Suchanek, MD., Ph.D.
stepan.suchanek@uvn.cz973208367
Backup ContactMichal Voska, MD.
michal.voska@uvn.cz773200360

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026