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Phase II study to evaluate the safety and efficacy of endoscopic radiofrequency ablation of the bile duct using the Habib Endo HPB catheter in patients with unresectable cholangiocarcinoma after biliary stent placement.

Not Applicable
Conditions
Cholangiocarcinoma
Registration Number
JPRN-UMIN000047127
Lead Sponsor
Yokohama City University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Patients in poor general condition who cannot undergo endoscopy (2) Patients taking more than 2 antiplatelet/anticoagulant drugs (3) Patients with a pacemaker implanted (4) Patients with a fever of 37.5 or higher and suspected cholangitis (5) Other patients deemed unsuitable for the procedure by the physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
All adverse events within 28 days after ERCP, including endoscopic RFA procedures
Secondary Outcome Measures
NameTimeMethod
RFA procedure success rate, stent patency after RFA, and overall survival
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