Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:21 PM
Ignite Modification Date:
2025-12-24 @ 9:21 PM
NCT ID:
NCT04782804
Eligibility Criteria:
Inclusion Criteria:
* Post R0 resection, pathologically confirmed intrahepatic cholangiocarcinoma.Patients were also pathologically confirmed to have any of the following high-risk factors (ie, positive resection margins, positive lymph nodes, positive perineural invasion, and intrahepatic cholangiocarcinoma \> 5cm in diameter;
* No history of any chemotherapy, radiotherapy, immunotherapy and interventional treatment prior to surgical resection;
* ECoG score 0-1 points;
* Liver function before medication child a, blood routine: WBC \> 2.5 \* 109 / L, PLT \> 60 \* 109 / L, coagulopathy: Pt prolonged \< 2S, ALT \< 150u / L;
* No heart, lung, or kidney function abnormalities were observed;
* No history of major bleeding disorders of the digestive tract;
* Signed informed consent;
Exclusion Criteria:
* Pregnant or lactating women.
* Patients with other malignant tumor.
* Patients with mental illness.
* Patients participated in other clinical trials in last three months.
* Residual lesions showed by Postoperative digital subtraction angiography(DSA).
* Postoperative patients treated with other targeted drugs, PD1 antibody and other immunotherapies, FOLFOX systemic chemotherapy, and HuaiErKeLi drug treatment
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT04782804
Study Brief:
Protocol Section:
NCT04782804