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Utility of Cholangioscopy After Stone Removal for Common Bile Duct Stones in Patients with Surgically Altered Anatomy

Utility of Cholangioscopy After Stone Removal for Common Bile Duct Stones in Patients with Surgically Altered Anatomy: A Single-Center Prospective Exploratory Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1030260094
Enrollment
10
Registered
2026-04-28
Start date
2026-04-28
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Common bile duct stone

Interventions

Use of cholangioscopy to confirm residual stones after stone removal

Sponsors

Watanabe Masafumi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients in whom common bile duct stones were identified on pre-procedural imaging (computed tomography, magnetic resonance cholangiopancreatography, ultrasonography, endoscopic ultrasonography, or balloon enteroscopy-assisted ERCP) and who were considered to require endoscopic stone removal. Patients with surgically altered anatomy (excluding Billroth I reconstruction). Patients with a distal bile duct diameter >=8 mm. Patients with a modified American Society of Anesthesiologists physical status (mASA-PS) classification of II or lower. Patients aged >=18 years who provided written informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: Patients in whom discontinuation of antithrombotic agents was considered difficult. Patients with cholangitis, severe jaundice (total bilirubin >5 mg/dL), or pancreatitis. Patients in whom single-session stone removal was considered difficult, including those with stacked stones, stones >15 mm in diameter, Mirizzi syndrome, or concomitant biliary stricture. Patients with a history of pancreatitis following balloon enteroscopy-assisted ERCP (BE-ERCP). Patients who were pregnant or possibly pregnant. Patients who were deemed unsuitable for participation in this study by the principal investigator or sub-investigators for medical or safety reasons.

Design outcomes

Primary

MeasureTime frame
Detection rate of residual stones by cholangioscopy

Secondary

MeasureTime frame
BE-ERCP-related adverse events

Contacts

Public ContactMasafumi Watanabe

Kitasato University Hospital

m.wata@kitasato-u.ac.jp+81-42-778-8111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026