Phase
Condition
Liver Cancer
Biliary Tract Cancer
Abdominal Cancer
Treatment
N/AClinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Obtention of a written informed consent.
Patient with histologically proved cholangiocarcinoma ; histologic diagnosis must be proved by biliary brushing, bile cytology, endobiliary biopsy under Spyglass, or by EUS-FNA.
Patient with Karnofsky score > 60, ECOG>level 2
Patient capable of fill in the quality of life questionnaire
For the first time treatment
CT, MRCP, EUS and other examinations indicate that the tumor has locally infiltrated large blood vessels and cannot be surgically removed
Exclusion Criteria
No written informed consent
Patients under or already treated by radiotherapy or chemotherapy treatment for cholangiocarcinoma.
Pregnant, parturient or breastfeeding women
Serious abnormalities in liver and kidney function and coagulation function
The ERCP guide wire cannot pass the stricture due to severe biliary stricture
Merge with other malignant tumors
Use other treatments that may affect the observation, such as radioactive particles or seed stent implantation, P53 injection, oral chemotherapy, interventional therapy, etc.
Study Design
Study Description
Connect with a study center
Hangzhou First People's Hospital
Hangzhou, Zhejiang 31006
ChinaSite Not Available

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