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Clinical Trial Summary

Short-acting coloration for normal liver protection in liver cancer patients undergoing radioembolization therapy a study on the effectiveness of all substances


Clinical Trial Description

Patients' liver function can be preserved when delivery of radioembolic agents to the non-tumorous liver is minimized. This is a single-center, single-arm clinical trial to evaluate the efficacy of short-acting embolization particles to temporarily embolize the hepatic arteries toward the non-tumorous liver in patients with hepatocellular carcinoma treated by radioembolization of a large perfused volume. A transient embolic effect will be evaluated by digital subtraction angiography during the procedure. Absorbed doses of the transiently protected non-tumorous liver and unprotected non-tumorous liver will be compared by pre-treatment SPECT-CT (99mTc injection without transient embolization) and post-treatment PET-CT (Y90 injection with transient embolization). In addition, liver volume and function changes for six months will be estimated using gadoxetic acid-enhanced dynamic MRI. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06229080
Study type Interventional
Source Next Biomedical Co., Ltd.
Contact Jin Woo Choi
Phone +82-32-454-4800
Email next@nextbiomedical.co.kr
Status Recruiting
Phase N/A
Start date March 15, 2023
Completion date December 31, 2024