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Digital SpyGlass Confirmed Common Bile Duct Stones Clearance Without Fluoroscopy

C

Chulalongkorn University

Status and phase

Completed
Phase 3

Conditions

Common Bile Duct Diseases
Stone - Biliary
Cholangitis, Sclerosing

Treatments

Procedure: Endoscopic Retrograde Cholangioscopy by SpyGlass (ERCS)

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02967926
791/2016

Details and patient eligibility

About

This study aim to evaluated the effectiveness of Digital SpyGlass Cholangioscopy to facilitate common bile duct stone removal without fluoroscopy

Full description

Patients This study recruited patients who suspected/confirmed CBDS from clinical manifestation, liver function tests and imaging studies. With CBD sized between 5 and 15 millimeters, which measured from transabdominal ultrasonography (US), computed tomography (CT), magnetic resonance cholangiopancreatography (MRCP) or endoscopic ultrasonography (EUS). The exclusion criteria were history of bile duct surgery, bile duct stricture, bile duct tumors, severe comorbid diseases, unstable vital signs, pregnancy, and coagulopathy. All patients were informed and wrote informed consent for the procedure.

Procedures Non-fluoroscopic CBDS removal was performed by experienced endoscopists, using standard side-viewing duodenoscope. After identified major papilla, the investigators performed bile duct cannulation with guidewire assisted technique. Successful cannulation confirmed by visualized bile aspiration. If the patients had difficult cannulation, double guidewire technique was used. After the successful bile duct cannulation, the investigators performed endoscopic standard sphincterotomy (EST). Precut sphincterotomy was not used in this study. Non fluoroscopic balloon extraction was performed. The balloon was pushed up to hilum then the investigators sweep until suspected complete CBD clearance. After that the investigators used digital SpyGlassTM to confirm the complete clearance of CBDS. If SpyGlassTM showed residual CBD stone, the investigators repeat balloon extraction. If SpyGlassTM showed complete clearance, the investigator proceed to perform final cholangiogram as reference standard for this study.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with clinically suspected/confirmed CBDS
  • CBD caliber 5-15 mm

Exclusion criteria

  • History of bile duct surgery
  • History of bile duct tumor
  • History of bile duct stricture
  • Severe comorbidity
  • Unstable vital signs
  • Pregnancy
  • Coagulopathy

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

51 participants in 1 patient group

ERCP without Fluoroscopy
Experimental group
Description:
Non-fluoroscopic common bile duct stone extraction
Treatment:
Procedure: Endoscopic Retrograde Cholangioscopy by SpyGlass (ERCS)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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