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The PROspera Kidney Transplant ACTIVE Rejection Assessment registry (ProActive) study
Description
This is a non-treatment study that uses a blood test ("Prospera") to measure kidney function following transplant. This study will look at the usefulness of the Prospera testing compared to the usual serum creatinine testing done at regular intervals in kidney transplant recipients.
MoreDetails
Age
Adult
Eligibility
Recent (within 60 days) kidney transplant recipient Age 18 or older Not on another monitoring study
Phase
Not Applicable - Describes studies without FDA-defined phases, including studies of devices or behavioral interventions.
Type of Study
Registry
Location
University of Colorado Hospital
Principal Investigator
Erik Stites
Study ID
Protocol Number: 19-2394
More information available at ClinicalTrials.gov: NCT04091984
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