Safety and Efficacy of Degradable Microsphere in Transcatheter Arterial Chemoembolization for Hepatocellular Carcinoma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19-79
SponsorNext Biomedical Co., Ltd.

About this trial

The purpose of this study was to prospectively collect clinical data from patients who underwent hepatic artery chemoembolization using microspheres with different degradation times (2 hours, 1 day, 2 weeks) based on standard treatment.

Eligibility criteria

Qualifiers

Adult patients aged 19 to 79 years

Patient who signed Informed Consent Form

Patients diagnosed with hepatocellular carcinoma by American Association for the Study of Liver Diseases (AASLD) and at least one of the following methods i. Magnetic resonance imaging (MRI) with early augmentation and delayed excretion of at least one solid liver lesion greater than 1 ㎝.

Patients should not be eligible for treatment by amputation or percutaneous resection or liver transplantation at the time of study enrollment.

Disqualifiers

Patients under the age of 19

Chronic kidney disease (CDK) grade 4 or 5 patients

Current or previous treatment with chemotherapy or radiation therapy or sorafenib or drug release chemoembolization (deTACE) after diagnosis of hepatocellular carcinoma

Extensive context-to-systemic shunts

Trial design

Treatments tested in this trial

  • Nexsphere™

Treatment groups

150 Participants
are divided into 1 treatment group

Sponsors and collaborators