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Search / Trial NCT02678013

RFA+Highly-purified CTL vs. RFA Alone for Recurrent HCC

Launched by MING KUANG · Feb 8, 2016

Trial Information

Current as of April 24, 2025

Unknown status

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. age 18-75 years;
  • 2. recurrence of HCC 12 months after initial hepatectomy;
  • 3. no other treatment received except for the initial hepatectomy;
  • 4. single tumor≤5.0cm in diameter; or 2-3 lesions each≤3.0cm;
  • 5. lesions visible on ultrasound and with an acceptable and safe path between the lesion and the skin as shown on ultrasound;
  • 6. no severe coagulation disorders (prothrombin activity\<40% or a platelet count\<40,000/mm3);
  • 7. Eastern Co-operative Oncology Group performance(ECOG) status 0-1.
  • Exclusion Criteria:
  • 1. Pregnant women, breastfeeding women or plan pregnancy for the future 2 years;
  • 2. The presence of vascular invasion or extrahepatic spread onimaging;
  • 3. Usage of strong immunosuppressive agents such as corticosteroids, cyclosporine A within six months or longer;
  • 4. HIV antibody or HCV antibody positive;
  • 5. Immunodeficiency diseases or autoimmune diseases (such as rheumatoid arthritis, Buerger's disease, multiple sclerosis and type 1 diabetes);
  • 6. Suffering with cancers (except skin cancer, prostate cancer or cervical carcinoma in situ) at the enrolling time or 5 years before;
  • 7. Suffering with other organ failure;
  • 8. Suffering with severe mental illness;
  • 9. Drug addiction (including alcohol) for 1 year before the enrolling time;
  • 10. Participate in other Clinical trials within three months prior to 3 months before the enrolling time;
  • 11. Other researchers believe that the patient is not fit for inclusion.

Trial Officials

Ming Kuang, Ph.D.

Principal Investigator

First Affiliated Hospital, Sun Yat-Sen University

About Ming Kuang

Ming Kuang is a dedicated clinical trial sponsor committed to advancing medical research and innovation. With a focus on developing novel therapeutic solutions, the organization collaborates with leading research institutions and healthcare professionals to conduct rigorous clinical trials. By prioritizing patient safety and ethical standards, Ming Kuang aims to facilitate the efficient progression of groundbreaking treatments from the laboratory to clinical practice, ultimately improving health outcomes and enhancing the quality of life for patients worldwide.

Locations

Guangzhou, Guangdong, China

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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