Narrow Band Imaging Versus White Light for the Detection and Miss of Sessile Serrated Lesion

NCT05684328 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 840

Last updated 2024-03-15

No results posted yet for this study

Summary

Narrow band imaging(NBI) could improve the detection of colorectal lesions, previous investigations demonstrated its potential in detecting not only colorectal adenoma but non-adenomatous polyps, including sessile serrated lesions. But no randomized controlled trials with NBI versus white light imaging(WLI) have been conducted to give a definitive conclusion with statistically significant differences. Therefore, we performed a multicenter, prospective, back to back, randomized controlled trial to compare sessile serrated lesions detection and miss rate of withdraw by NBI and WLI in colonoscopy.

Conditions

  • Colorectal Sessile Serrated Lesion

Interventions

PROCEDURE

WLI Then NBI Withdrawal

Patients in WLI then NBI withdrawal group will first be carefully inspected by white light imaging(WLI), each polyp found should be removed. According to the ESGE guideline of colorectal polypectomy, the lesions which size between 4-9mm should by removed by cold snare. Cold biopsy forceps could be utilized considering the difficulty in resection of flat and diminutive polyps(size ≤ 3mm). Then change to narrow band imaging(NBI) for the second withdraw to detect the lesions which found in second time but not the first.

PROCEDURE

NBI Then WLI Withdrawal

Patients in NBI then WLI withdrawal group will first be carefully inspected by narrow band imaging(NBI), each polyp found should be removed. According to the ESGE guideline of colorectal polypectomy, the lesions which size between 4-9mm should by removed by cold snare. Cold biopsy forceps could be utilized considering the difficulty in resection of flat and diminutive polyps(size ≤ 3mm). Then change to white light imaging(WLI) for the second withdraw to detect the lesions which found in second time but not the first.

Sponsors & Collaborators

  • The First Affiliated Hospital of Dalian Medical University

    collaborator OTHER
  • The Second Hospital of Hebei Medical University

    collaborator OTHER
  • Yantaishan Hospital

    collaborator UNKNOWN
  • The Second Affiliated Hospital of Guangzhou University of Chinese Medicine

    collaborator UNKNOWN
  • 900 Hospital of Joint Logistics Support Force of PLA

    collaborator OTHER
  • Heilongjiang provincial hospital

    collaborator UNKNOWN
  • Ankang Central Hospital

    collaborator OTHER
  • Nongken Jiansanjiang People Hospital of Heilongjiang Province

    collaborator UNKNOWN
  • Huadong Hospital

    collaborator OTHER
  • The Second Affiliated Hospital of Baotou Medical College

    collaborator OTHER
  • Qilu Hospital, Shandong University

    collaborator UNKNOWN
  • Shandong First Medical University

    collaborator OTHER
  • Air Force Military Medical University, China

    collaborator OTHER
  • Tengzhou Central People's Hospital

    collaborator OTHER_GOV
  • Chongqing General Hospital

    collaborator OTHER
  • Haikou People's Hospital

    collaborator OTHER
  • Changhai Hospital

    lead OTHER

Principal Investigators

  • Zhaoshen Li, MD · Changhai Hospital

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
45 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-01
Primary Completion
2024-03-28
Completion
2024-05-28

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05684328 on ClinicalTrials.gov