End-Stage Renal Disease Clinical Trial
Official title:
Prospective, Randomized, Double-Blind, Double-Dummy, Multicenter Trial to Assess Safety of Single Dose vs. Traditional Administration of Thymoglobulin Induction for Renal Transplantation
In a non-blinded pilot study conducted at the University of Nebraska Medical Center, evidence was found that a single large dose of Thymoglobulin on the day of kidney transplantation produced better kidney function than the standard dosing plan, when the same amount is divided into smaller doses on 4 days. This new study repeats that dose comparison, but with double-blinding and at multiple transplantation centers.
This study is designed to confirm the one-year safety of single-dose rabbit anti-thymocyte
globulin induction at kidney transplantation, compared to the conventional administration of
the same overall dose divided into four smaller doses across four days. Two randomized
groups of kidney transplant recipients will be each administered the drug Thymoglobulin
according to a different dosing regimen. The control group will receive the usual and
traditional regimen of a total of 6 mg/Kg divided into 4 doses, 1 on the day of
transplantation and 1 each day on the next 3 days. The experimental group will receive the
same total Thymoglobulin dose, 6 mg/Kg, but entirely on the day of transplantation.
The study will be double-blinded, with placebo doses of Thymoglobulin administered as needed
to enrollees in the experimental group. Enrollment is targeted at 165, with 150 subjects
needed to complete the study for adequate evaluation.
;
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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