Study to Evaluate Safety and Immunologic Biomarker of Rapamune in Patients With Stable Renal Transplant Recipient
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ClinicalTrials.gov Identifier: NCT01592253
Recruitment Status : Unknown
Verified June 2012 by ChulWoo Yang, Seoul St. Mary's Hospital. Recruitment status was: Recruiting
For patients who meet the inclusion criteria and who agree to participate in this study, the investigators sampled peripheral blood 10cc and performed the analysis for immunologic profile just before the conversion of immune suppressant. At 1 month, 6 month, and 1 year from the conversion of Immune suppressant (CNI to rapamune), the investigators performed tha analysis fo immune profile again. During the study period, the interval of the visit of subclinic and the kinds of laboratory test (Blood and urine test) would not change compared to before the start of this study.
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Ages Eligible for Study:
Child, Adult, Older Adult
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Renal transplant recipient who has passed at least 10 years
No acute rejection episode during the previous 6 months
No change of prescription of immune suppressants
Normal allograft function (MDRD eGFR > 80 mL/min/1.73 m2)
Change of allograft function less than 10 % of baseline value durant the previous 1 year
No proteinuria and hematuria
Patients who donut want to participate in this study
Patients who should continue immune suppressant due to another cause (e/g combined autoimmune disease)