The major aim of this research study is to investigate the relationship between genetic variation in DNA (inherited code material in the cells of the body) and factors affecting transplant outcomes, like the drugs people receive or the way their immune systems work, for example. To do this, investigators will collect blood samples from participants. Genetic material will be separated from each blood sample and analyzed, looking for genetic variation.
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Transplant recipient genotypes: time to chronic graft disfunction
Timeframe: Day 0 to Year 5
Transplant recipient genotypes: time to a persistent 25% decrease in Estimated Glomerular Filtration Rate (eGFR)
Timeframe: Day 0 to Year 5
Transplant recipient genotypes: time to acute rejection
Timeframe: Day 0 to Year 5
Transplant recipient genotypes: time to allograft failure
Timeframe: Day 0 to Year 5
Donor Genotypes: time to chronic graft dysfunction
Timeframe: Day 0 to Year 5
Donor Genotypes: time to a persistent 25% decrease in eGFR
Timeframe: Day 0 to year 5
Donor Genotypes: time to allograft failure
Timeframe: Day 0 to Year 5
Recipient genotypes: time to select mycophenolate-related toxicities (leukopenia, anemia)
Timeframe: Day 0 to Year 5
Recipient genotypes: time to select Calcineurin Inhibitor (CNI)-related toxicities
Timeframe: Day 0 to Year 5
Recipient genotypes: repeated measures of clinically obtained tacrolimus trough blood levels
Timeframe: Day 0 to Year 5
Recipient candidate genotypes: Calcineurin (CN) and IMPDH protein activity and expression
Timeframe: Day 0 to Year 5