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Recruiting NCT06097637

Underwater Endoscopic Mucosal Resection Versus Metal Clips With Hot Snare Polypectomy for Resection of Big Pedunculated Colorectal Polyps

No phase Interventional Pedunculated Colorectal Polyps Haemorrhage

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: underwater endoscopic mucosal resection, hot snare polypectomy.
Who it may be relevant to
Registry conditions: Pedunculated Colorectal Polyps, Haemorrhage. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Underwater Endoscopic Mucosal Resection Versus Metal Clips With Hot Snare Polypectomy for Resection of Big Pedunculated Colorectal Polyps: A Randomized Controlled Trial

Overview

Endoscopic resection of pedunculated polyps mainly focuses on how to prevent bleeding, and also needs to pay attention to the convenience of resection and the integrity of resection, which means that different endoscopic resection strategies should be adopted for pedunculated polyps with different pedicle sizes. The head larger than 20mm or pedicle larger than 5mm are defined as large pedunculated polyps, which are at greater risk of bleeding. Current guidelines recommend hot removal by snare following preoperative saline injection, ligation of the pedicle with a nylon ring or metal clip, depending on the size of the polyp head and pedicle. However, the use of snares and metal clamps does not appear to reduce delayed postoperative bleeding, and the technical requirements of nylon ligation are relatively high. Recent studies have found that Underwater endoscopic mucosal resection (UEMR) is also safe and effective for the treatment of large and medium colorectal sessile polyps. Therefore, it is still necessary to further explore new safe and effective endoscopic resection strategies and techniques.

Interventions

  • Other underwater endoscopic mucosal resection
    underwater endoscopic mucosal resection achieves similar rates of complete resection with comparable safety, with lower rates of recurrence and fewer repeat procedures.
  • Other hot snare polypectomy
    Current guidelines recommend preoperative hot snare polypectomy after preoperative saline injection, nylon ring, or metal clip ligation of the tip and pedicle of the polyps

Primary outcome measures

  • Prevalence of immediate bleeding [Time frame: 1 Minutes]
Secondary outcome measures (1)
  • delayed hemorrhage [Time frame: 2 weeks and 4 weeks]

Eligibility criteria

Inclusion criteria

  • Patients undergoing endoscopic resection of small and medium pedicled polyps in the First Affiliated Hospital of Ningbo University from October 2023 to August 2026;
  • Age 18-75 years old;
  • Patients who voluntarily agreed to participate in this study and signed informed consent.

Exclusion criteria

  • Persons under 18 years of age
  • Persons unwilling or unable to provide informed consent
  • Treatment or radiotherapy for malignant diseases, severe chronic heart or lung diseases, coronary or cerebrovascular events requiring hospitalization within the last 3 months
  • Malignant polyps have infiltrated the pedicle
  • Abdominal symptoms such as severe abdominal pain, abdominal distension, and nausea
  • Patients with inadequate intestinal preparation
  • Patients with lifelong anticoagulant therapy or severe bleeding diseases, patients who have recently taken anticoagulant drugs or antiplatelet drugs (within 1 week)
  • Pregnant or lactating

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

China · 1 center
  • the First Affiliated Hospital of Ningbo University — Ningbo

Identifiers

NCT: NCT06097637 · 2023-139A-YJ01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗