None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients 20 years of age or older, who voluntarily agree to participate in the study and sign the informed consent. 2.Patients with cytopathologically diagnosed inoperable extrahepatic cholangiocarcinoma
Exclusion criteria
Exclusion criteria: 1.Patients who refuse to sign the informed consent 2.Patients with metastatic cancer (stage IV) or malignant ascites 3.Patients with intrahepatic cholangiocarcinoma 4.Patients who are unable to undergo endoscopic procedures as determined by the investigator. 5.Patients with a life expectancy of 3 months or less 6.Patients with ID-RFA contraindications: pacemaker, pregnancy, uncorrected bleeding tendency (PT INR > 1.5, platelets < 50,000/mm3)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 2-year local control rate | — |
Secondary
| Measure | Time frame |
|---|---|
| 1-year local control rate;Overall survival;Progression-free survival;Local progression-free survival;Period of Stent patency | — |
Countries
Korea, Republic of
Contacts
National Cancer Center