Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Miami, Florida 33176


Purpose:

The objective of this study is to evaluate feasibility and safety of the adoptive transfer of activated natural killer (NK) cells extracted from cadaveric donor liver graft perfusate for liver transplant recipients with hepatocellular carcinoma (HCC)


Criteria:

Inclusion Criteria: - Primary liver transplant recipient with HCC - Patients need to meet the liver transplant eligibility criteria - Cardiac function; cardiac echo will indicate that ejection fraction (EF) > 35% or right ventricular systolic pressure (RVSP) < 50mmHg. Stress echo will show no ischemic lesion (if applicable). - Pulmonary function; SpO2 >90% or PaO2 > 60 mmHg, or CT will show no active pulmonary lesion. - Complete blood count; Platelet > 20,000 /mm3, Hematocrit > 20%, WBC > 1,000 /mm3 - Eighteen years of age or older - Ability to provide informed consent - If female of childbearing potential: Must not be lactating, must have a negative serum B-human chorionic gonadotropin (HCG) test within 7 days prior to Day of Transplant, and must agree to practice an acceptable and reliable form of contraception during the study Ability to provide informed consent Exclusion Criteria: - Living donor liver transplant; a healthy person donates part of his or her liver to the recipient - Multiple organ transplants - Prior solid organ or bone marrow transplant recipients - Fluminant hepatic failure - The patients regularly receive the hemodialysis more than twice a week before liver transplant - Status 1 transplants; acute severe disease and defined as a patient with only recent development of liver disease who is in the intensive care unit of the hospital with a life expectancy without a liver transplant of fewer than 7 days - ABO incompatible transplants - Transplants utilizing livers from non-heart beating donors; the cardiac death donor - Recipients of investigational therapy within 90 days prior to transplant procedure - Acute viral illness - History of malignancy within 5 years, with exception of: Adequately treated localized squamous or basal cell carcinoma of the skin without evidence or recurrence, and/or Hepatocellular carcinoma - Illness other than primary liver disease (e.g., severe ischemic heart disease, left ventricular dysfunction, or pulmonary disease), which, in the opinion of the Investigator, may significantly increase the risk of the transplantation procedure - Current drug or alcohol abuse or, in the opinion of the Investigator, is at risk for poor compliance (no drug testing required) - Serology positive donor (HCV, HBsAg, HBcAb, HTLV-1, HTLV-3, EBVIgM) - Poor liver function donor (Total bilirubin > 3.0 mg/dl, Prothrombin time > 35 sec), - Patients who receive intercurrent chemotherapy at the time of enrollment


NCT ID:

NCT01147380


Primary Contact:

Principal Investigator
Seigo Nishida, MD PhD
Department of Surgery, University of Miami


Backup Contact:

N/A


Location Contact:

Miami, Florida 33176
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.