Clinical trial · Interventional
Drug-loadable(T-ACE Beads)for Hepatoma Embolization Therapy
Hydrophilic Radiopaque Microsphere With Doxorubicin for Hepatoma Embolization Therapy
NCT03299036CI-TRIAL-00035401completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to evaluate the safety and efficacy of Radiopaque Microsphere (T-ACE Beads with doxorubicin) interventional therapy for patients with liver cancer
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer of Liver | Malignant Liver Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Taiwan ACE Beads with doxorubicin | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Taiwan ACE Beads with doxorubicin
- description
- The use of Taiwan ACE Beads (T-ACE) microspheres embolization with doxorubicin as a treatment for patients with hepatoma.
- interventionNames
- Device: Taiwan ACE Beads with doxorubicin
Primary outcomes (2)
- measure
- Patients Survival (Safety)
- timeFrame
- An average of 12 weeks.
- description
- Survival rate will be evaluated since treatment day until the date of death or final observation.
- measure
- Tumor response in patients with hepatoma who received Taiwan ACE beads (TACE) microspheres embolization evaluated with mRECIST criteria
- timeFrame
- Three months
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
Show eligibility criteria text
Inclusion Criteria: Patients must meet all of the following inclusion criteria in order to be entered into the study: A. Both genders of patients age 20 or older. B. Patients diagnosed of liver cancer (MUST meet at least ONE of the following criteria:) 1. Diagnosed via tumor biopsy by Pathologists, and confirmed by on-service physician. 2. High risk patients (Viral hepatitis B or C or cirrhotics) with typical liver cancer image appeared on more than two radiographic examinations (Ultrasound, MRI, CT scan or Angiography). 3. High risk patients (Viral hepatitis B or C cirrhotics) with evidence of enlarging image of liver cancer via more than two follow-up records. C. In intermediate stage by BCLC staging, tumor size under 8 centimeters, with liver function at Child-Pugh class ≤ 8, and is either difficult to accept an operation or reluctant to accept any operation. D. Disease can be treated by transarterial chemoembolization, and can be evaluated by Ultrasound, Magnetic resonance imaging (MRI), or computed tomography (CT). E. Performance status ECOG 2 or less. Patient has a life expectancy of at least 3 months. Exclusion Criteria: If patients meet any of the following criteria they may not be entered into the study: A. major branch of portal vein has been invaded already; extrahepatic metastasis or the the other malignant tumors. B. Evidences of decompensation: Total Bilirubin\>2, PT prolong\>3 seconds, Child-Pugh class\>8, refractory ascites, active bleeding, hepatic encephalopathy, and severe infection. C. Tumor size (diameter) larger than 8 centimeters. D. Not on dialysis with Creatinine \>2.0 mg/dL. E. Allergic to iodine or other injections. F. Other main organ failure (Heart, Lung, or Kidney). G. WBC\<3000, or Platelet Count \<50,000 mg/dL. H. Performance status ECOG of 3 or more. I. Pregnant women and breath feeding women. J. Patients whose blood vessel are too difficult to do Taiwan ACE Beads procedure. K. Prominent AV shunt. L. Severe atherosclerosis. M. Vasospasm or possible major vascular injury. N. Arteriovenous shunt patients, diameter larger than the size of microsphere available. O. Collateral vascular exists and may endanger non-targeted area during arterial chemoembolization. P. Contraindications for doxorubicin. Q. Numerous of tumors locate at different lobes, high risk of Hepatic insufficiency. R. Unwilling to sign a written informed consent form. S. Allergic to pharmaceutical excipients related to Microspheres.
References
Publications (2)
- BACKGROUNDLiu YS, Lin XZ, Tsai HM, Tsai HW, Chen GC, Chen SF, Kang JW, Chou CM, Chen CY. Development of biodegradable radiopaque microsphere for arterial embolization-a pig study. World J Radiol. 2015 Aug 28;7(8):212-9. doi: 10.4329/wjr.v7.i8.212. PMID 26339465
- BACKGROUNDLiu YS, Ou MC, Tsai YS, Lin XZ, Wang CK, Tsai HM, Chuang MT. Transarterial chemoembolization using gelatin sponges or microspheres plus lipiodol-doxorubicin versus doxorubicin-loaded beads for the treatment of hepatocellular carcinoma. Korean J Radiol. 2015 Jan-Feb;16(1):125-32. doi: 10.3348/kjr.2015.16.1.125. Epub 2015 Jan 9. PMID 25598680