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Clinical Trials/NCT07759960
NCT07759960RecruitingNot Applicable

Underwater Endoscopic Mucosal Resection Versus Endoscopic Submucosal Dissection for the Treatment of Small Rectal Neuroendocrine Tumors: A Prospective, Multicenter, Non-inferiority Trial

Nanfang Hospital, Southern Medical University1 site in 1 country174 target enrollmentStarted: April 14, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
174
Locations
1
Primary Endpoint
histological complete resection

Study Overview

Brief Summary

Underwater endoscopic mucosal resection (UEMR) and endoscopic submucosal dissection (ESD) have both been reported to be two effective treatment methods for small rectal neuroendocrine tumor (NET). However, there is no consensus on the best method for the endoscopic resection of rectal NET. Therefore, we aimed to compare the efficacy and safety of UEMR and ESD for the treatment of small rectal NET.

Detailed Description

Researchers plan to conduct a prospective, multicenter, non-inferiority, randomized controlled trial to compare the efficacy and safety of UEMR and ESD for the treatment of small rectal NET in ten endoscopic centers in China.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age from 18 to 75 years;
  • •With a high suspicion or evidence of rectal NET assessed using EUS, CT scan or colonoscopy;
  • •With tumor size ≤10 mm assessed by colonoscopy or EUS;
  • •Plan to receive UEMR or ESD treatment and provide written informed consent.

Exclusion Criteria

  • •Unable to tolerate ESD or UEMR as assessed by the research team;
  • •Complicated with serious diseases such as malignant tumor, which may lead to shorter life expectancy, the research team considers that it is not suitable for inclusion in the study after comprehensive evaluation;
  • •Rectal NET with lymph node metastasis or distant metastasis;
  • •Received resection of rectal neuroendocrine tumor by other surgical procedures;
  • •Multiple rectal neuroendocrine tumors;
  • •Vulnerable groups such as pregnant women or patients with mental disorders;
  • •Poor compliance, unable to cooperate with treatment.

Arms & Interventions

UEMR group

Experimental

In UEMR group, enrolled patients will receive UEMR to remove small rectal NET.

Intervention: UEMR procedure (Procedure)

ESD group

Active Comparator

In ESD group, enrolled patients will receive the standard treatment modality of ESD to remove small rectal NET

Intervention: ESD procedure (Procedure)

Outcomes

Primary Outcomes

histological complete resection

Time Frame: within 14 days after procedure

complete single-piece (en bloc) resection of the targeted lesion with horizontal and vertical free margins.

Secondary Outcomes

  • length of stay(within 14 days after procedure)
  • success rate of operation(intraoperative)
  • en bloc resection(intraoperative)
  • operation time(intraoperative)
  • complications(within 14 days after procedure)
  • operation cost(within 14 days after procedure)
  • hospitalization cost(within 14 days after procedure)
  • histopathologic grade(within 14 days after procedure)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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