Fact CheckerSign in

NCT06901856Not yet recruiting

Endoscopic Resection for Small Rectal Neuroendocrine Tumors

Modified Cap-assisted Endoscopic Mucosal Resection and Modified Endoscopic Mucosal Resection with a Ligation Device for Small Rectal Neuroendocrine Tumors Less Than 1 Cm: a Muticenter Randomized Noninferiority Trial

Source: ClinicalTrials.gov · Last updated 30 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

According to clinical practice and relevant retrospective research data, both modified cap-assisted endoscopic mucosal resection (mEMR-C) and endoscopic mucosal resection with a ligation device(ESMR-L) were reported to be effective for the treatment of small rectal neuroendocrine tumors (NETs) . However, there is a lack of multicenter prospective studies to evaluate the advantages and disadvantages of mEMR-C and mEMR-L. mEMR-C is the modified ESMR-L without submucosal injection.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
120 (estimated)
First submitted
24 Mar 2025
Start date
Mar 2025
Primary completion date
Dec 2025
Lead sponsor
Guangdong Provincial People's Hospital
NCT number
NCT06901856

What you commit to

  • Study type: Interventional
  • Planned participants: 120
  • From Mar 2025 to the primary completion date, Dec 2025
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Received resection of rectal neuroendocrine tumor by other surgical procedures;

Other illness

  • 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;
  • Vulnerable groups such as pregnant women or patients with mental disorders;

Other

  • Unable to tolerate mEMR-L or mEMR-C as assessed by the research team of each center;
  • Rectal NET with lymph node metastasis or distant metastasis;
  • Multiple rectal neuroendocrine tumors;
  • Poor compliance, unable to cooperate with treatment.

Who the study is looking for

  • Age from 18 to 80 years;
  • With a high suspicion or evidence of rectal NET assessed using EUS or colonoscopy;
  • With tumor size ≤10 mm assessed by colonoscopy;
  • Plan to receive mEMR-C or mEMR-L treatment and provide written informed consent;

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.