Actively Recruiting

Phase Not Applicable
Age: 20Years +
All Genders
NCT06168292

Intraductal Radiofrequency Thermoablation and Radiotherapy Combined Treatment for Extrahepatic Cholangiocarcinoma

Led by National Cancer Center, Korea · Updated on 2025-06-19

53

Participants Needed

1

Research Sites

325 weeks

Total Duration

On this page

Sponsors

N

National Cancer Center, Korea

Lead Sponsor

B

Boston Scientific Corporation

Collaborating Sponsor

AI-Summary

What this Trial Is About

\[Study objectives\] To evaluate the efficacy and safety of the combined treatment of radiotherapy and endoscopic intraductal radiofrequency ablation in patients with locoregional extrahepatic cholangiocarcinoma.

CONDITIONS

Official Title

Intraductal Radiofrequency Thermoablation and Radiotherapy Combined Treatment for Extrahepatic Cholangiocarcinoma

Who Can Participate

Age: 20Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 20 years of age or older who voluntarily agree to participate and sign informed consent
  • Patients with cytopathologically diagnosed inoperable extrahepatic cholangiocarcinoma
Not Eligible

You will not qualify if you...

  • Patients who refuse to sign informed consent
  • Patients with metastatic cancer (stage IV) or malignant ascites
  • Patients with intrahepatic cholangiocarcinoma
  • Patients unable to undergo endoscopic procedures as determined by the investigator
  • Patients with a life expectancy of 3 months or less
  • Patients with contraindications to ID-RFA such as pacemaker, pregnancy, or uncorrected bleeding tendency (PT INR > 1.5, platelets < 50,000/mm3)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

National Cancer Center, Korea

Goyang-si, Other, South Korea, 10408

Actively Recruiting

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Research Team

S

Sang Myung Woo, M.D

CONTACT

J

Jung Won Chun, M.D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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