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:
2025-12-25 @ 3:39 AM
Ignite Modification Date:
2025-12-25 @ 3:39 AM
NCT ID:
NCT02634502
Eligibility Criteria:
Inclusion Criteria:
* Karnofsky Performance Status ≥ 70
* Histologically/cytologically confirmed pancreatic adenocarcinoma.
* Patients must have underwent radical resection of the pancreatic lesion, or have their locally advanced pancreatic lesion controlled after first-line chemotherapy.
* At least one measurable liver metastasis by RECIST criteria must be present.
* Single liver metastasis smaller than 5cm, or multiple liver metastases less than 6 lesions and smaller than 3cm for each, without metastasis to other sites.
* Patients must have adequate organ functions reflected by the laboratory criteria below:
Granulocytes ≥ 2,000/uL, Hemoglobin ≥ 8.0 gm/dL, Platelets ≥ 100,000/uL, Serum creatinine \< 2.0 mg/dL, Bilirubin \< 1.5 mg/dL, SGPT \< 2.5 x normal, prothrombin time \<13.5s
* Prior therapy, e.g., chemotherapy, radiation, is allowed provided that at least 4 weeks washout time is given.
* Patients with jaundice must have a biliary drainage decompression operation before recruitment.
* Ability to understand and the willingness to sign a written informed consent.
Exclusion Criteria:
* Prior treatment with S-1.
* Liver metastatic lesion is located at the surface of the liver, with more than 1/3 of the tumor protruding outside.
* Subject has Child-Pugh grade Class C hepatic impairment, massive ascites, active gastrointestinal bleeding, severe coagulation disorder that could not be corrected, or other contraindication for radiofrequency ablation.
* Tumor invasion of Cavity organs.
* Known central nervous system involvement and leptomeningeal disease.
* Concurrent infection requiring intravenous antibiotics.
* Other serious illness or condition including cardiac disease including congestive heart failure (New York Heart Association Classification III or IV), active HIV infection/HIV disease, psychiatric disorders.
* Subject has previous or concurrent cancer that is distinct in primary site or histology from pancreatic adenocarcinoma except cervical carcinoma in situ, non-melanoma carcinoma of the skin or in situ carcinoma of the bladder. Any cancer curatively treated greater than 3 years prior to entry is permitted.
* Pregnant or lactating women.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT02634502
Study Brief:
Protocol Section:
NCT02634502