Expired Study
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Cincinnati, Ohio 45219


Purpose:

To determine how safe and effective giving Thymoglobulin before transplantation to patients who are going to be receiving kidney transplants.


Study summary:

We will evaluate the therapeutic efficacy of administering Thymoglobulin® induction pre-transplantation in renal allograft recipients. Patients receiving pre-transplant Thymoglobulin will be evaluated for acute rejection (Banff '97 criteria), survival, and safety at 6 months. Overall the use of Thymoglobulin induction pre-transplantation will be safe and effective.


Criteria:

Inclusion Criteria: 1. Adult living donor renal transplant recipient. 2. Patient is at least 18 years of age 3. If female and of childbearing potential, have a negative serum or urine HCG within 24 hours prior to Study Day -5 (Day of 1st Thymoglobulin dose) and must practice a medically approved method of birth control for the past 30 days prior to enrollment and agree to continue this practice during the 6 month efficacy analysis. 4. Signed informed consent. Exclusion Criteria: 1. Human Leukocyte Antibody (HLA) identical living donor transplant recipient. 2. History of a positive cross-match with the donor. 3. Patients with a peak CDC PRA > 50% or a current CDC PRA > 25%. 4. Patients who have previously received a kidney transplant. 5. Active donor or recipient serology positive for human immunodeficiency virus (HIV), Hepatitis B virus (HBV), or Hepatitis C virus (HCV). 6. History of noncompliance. 7. History of chronic corticosteroid or immunosuppressive use except for inhaled corticosteroids to treat asthma. . 8. Multiple organ transplant recipient. 9. Patient with a urinary bladder that is absent or not functional (e.g. self catheterization) pretransplant. 10. Patient who does not agree to use effective birth control during the 6-month efficacy analysis. 11. Known contraindication to administration of rabbit antithymocyte globulin. 12. Initial screening laboratory evaluations will be done locally before renal transplantation and the following laboratory values will be exclusionary: Platelets < 100,000/mm23 or WBC < 3000/mm3 13. Currently abusing drugs or alcohol or, in the opinion of the investigator, is at high risk for poor compliance. 14. Patient who, in the opinion of the investigator, has significant medical or psychosocial problems or unstable disease states that would preclude participation in the study. Examples of significant problems include, but are not limited to, morbid obesity or severe cardiac disease. -


NCT ID:

NCT00771745


Primary Contact:

Principal Investigator
E. Steve Woodle, MD
University of Cincinnati


Backup Contact:

N/A


Location Contact:

Cincinnati, Ohio 45219
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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