Screening Single-operator Cholangioscopy for Neoplastic Bile Duct Lesions

Sponsor
Soonchunhyang University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05600803
Collaborator
(none)
236
1
36
6.6

Study Details

Study Description

Brief Summary

This is the prospective observational study to explore whether the SpyGlass DS II system could be used to screen early-stage neoplastic bile duct lesions in selected patients.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Single-operator cholangioscopy

Detailed Description

It is difficult to diagnose neoplastic bile duct lesions (including cholangiocarcinomas) via direct endoscopic evaluation of the bile duct. Most evaluations of biliary lesions have used indirect imaging modalities such as CT, MRI, or ERCP. However, CT and MRI do not yield tissue diagnoses, unlike ERCP, although the diagnostic accuracy for the latter remains unsatisfactory. Recently, remarkable advances in cholangioscopic systems have been made. Of the currently available cholangioscopic systems, the SpyGlass (Boston Scientific Co, Natick, Mass, USA) is a disposable cholangioscope permitting 4-way deflected steering by a single operator. We aimed to evaluate the efficacy of single-operator cholangioscopy (SpyGlass DS II system) to screen for neoplastic bile duct lesions in patients with bile duct stones, which is one of the risk factor of cholangiocarcinoma.

Study Design

Study Type:
Observational
Anticipated Enrollment :
236 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Efficacy of Single-operator Cholangioscopy to Screen for Neoplastic Bile Duct Lesions in Patients With Bile Duct Stones
Anticipated Study Start Date :
Oct 30, 2022
Anticipated Primary Completion Date :
Oct 30, 2024
Anticipated Study Completion Date :
Oct 30, 2025

Arms and Interventions

Arm Intervention/Treatment
DSOC group

Study subjects are patients who satisfied the inclusion/exclusion criteria and underwent single-operator cholangioscopy.

Procedure: Single-operator cholangioscopy
SpyGlass (Boston Scientific Co, Marlborough, USA) which enabled the direct visualization of the pancreaticobiliary system for the evaluation of intraductal lesions

Outcome Measures

Primary Outcome Measures

  1. detection rate [Until the end of the single-operator cholangioscopy session (up to 20 minutes)]

    detection rate of intraductal neoplastic lesions in patients with bile duct stones who underwent single-operator cholangioscopy

Secondary Outcome Measures

  1. Technical success of cholangioscopy [Up to 15 minutes from the time the endoscope passes through the oral cavity]

    successful insertion of the cholangioscope through the ampulla of Vater and advancement up to the bifurcation of the biliary tree

  2. Technical success of cholangioscopy-guided biopsy [Until the end of the single-operator cholangioscopy session (up to 20 minutes)]

    successful tissue sampling of intraductal superficial lesions under direct visualization

  3. Adverse events [From the start of endoscopy to the end of the study observation period (at least 12 months)]

    all adverse events including cholangitis, pancreatitis, perforation, bleeding, and air embolism based on ASGE criteria

  4. Number needed to screen [From the start of endoscopy to the end of the study observation period (at least 12 months)]

    the number of persons who would need to be screened to diagnose one neoplastic bile duct lesion in selected patients

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Aged > 18 years

  2. Patients with risk factors for CCA (viral hepatitis, parasitic infection, choledochal cyst, primary sclerosing cholangitis, biliary stones, and toxins)

  3. Patients who undergo ERCP for confirmation of CBD clearance

  4. Dilated common bile duct (> 10 mm)

  5. Previous sphincteroplasty, such as major endoscopic sphincterotomy and/or endoscopic papillary balloon dilatation

Exclusion Criteria:
  1. Presence of biliary tract cancer

  2. Presence of distal CBD stricture

  3. Bleeding tendency (INR>1.5 or platelets <50000 mm3)

  4. Contraindications of ERCP

Contacts and Locations

Locations

Site City State Country Postal Code
1 Soonchunhyang University Bucheon Hospital Bucheon Gyeonggi-do Korea, Republic of 14584

Sponsors and Collaborators

  • Soonchunhyang University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jong Ho Moon, MD, PhD, FASGE, FJGES, Soonchunhyang University Hospital
ClinicalTrials.gov Identifier:
NCT05600803
Other Study ID Numbers:
  • screeningsoc
First Posted:
Nov 1, 2022
Last Update Posted:
Nov 1, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 1, 2022