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 @ 4:27 AM
Ignite Modification Date:
2025-12-25 @ 4:27 AM
NCT ID:
NCT02960620
Eligibility Criteria:
Inclusion Criteria:
* Patients will be recruited from the patient population referred to the principal clinician for regional liver cancer therapy.
* Potential candidates are those diagnosed with primary or secondary liver neoplasia. The histopathology confirmation criterion may be waived in patients with a radiographically identifiable liver mass, known laboratory or clinical risk factors for cancer or elevated tumor markers and clinical findings. Guidelines from the American Association for the Study of Liver Diseases (AASLD) and the European Association for the Study of the Liver (EASL) describe in detail the approach and algorithm for diagnosing Hepatocellular Carcinoma (HCC).
* Eastern Cooperative Oncology Group (ECOG) Performance Status Score 0 - 2
* Life expectancy ≥ 3 months
* \> 4 weeks since prior radiation, surgery or chemotherapy
* Able to comprehend and provide consent in accordance with institutional and federal guidelines
Exclusion Criteria:
* Any other liver therapy planned for cancer treatment
* Uncorrectable flow to the gastrointestinal tract
* Estimated radiation doses to the lungs greater than 30 Gy in a single administration or 50 Gy in multiple administrations
* Significant extrahepatic disease representing imminent life-threatening outcome
* Pregnancy
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02960620
Study Brief:
Protocol Section:
NCT02960620