Trial to Define the Benefits and Harms of Deceased Donor Kidney Procurement Biopsies



Status:Not yet recruiting
Conditions:Renal Impairment / Chronic Kidney Disease, Renal Impairment / Chronic Kidney Disease
Therapuetic Areas:Nephrology / Urology
Healthy:No
Age Range:18 - Any
Updated:3/1/2019
Start Date:April 2019
End Date:April 2022
Contact:Craig J Dedert, BSN
Email:craig.dedert@health.slu.edu
Phone:314-577-8461

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Pilot Randomized Trial to Define the Benefits and Harms of Deceased Donor Kidney Procurement Biopsies

The purpose of this research study is to compare the impact of the availability of biopsy
results at the time of organ offers on the use and outcomes of kidneys from deceased donors.

Randomization of biopsy processing will be performed at the level of the deceased donor.

If the participant agrees to be in this study and signs the informed consent, at the time
that a kidney is accepted for them, the accepted deceased donor will be randomized, like a
flip of a coin, to one of two groups.

- Group 1: biopsies will be processed immediately (routine "frozen section") and results
will be available to clinical teams at the time of the organ offers. Frozen section
refers to a process where tissue from the biopsy sample is prepared by freezing and then
slicing the tissue sample. Importantly, it can be done in about 15 to 20 minutes. Frozen
sections are done when an immediate answer is needed; however, the quality of the sample
is not always optimal.

- Group 2: biopsies will be processed using "permanent sections" - these results will not
be available until after the organ is transplanted. Permanent section refers to a
process where tissue from the biopsy sample is prepared by placing the tissue sample in
a fixative, called formalin, to preserve the tissue, processing it through other
additional solutions, and then placing it in paraffin wax. After the wax hardens, the
tissue is cut into very thin slices, which are placed on slides and stained. This
process normally takes several days.

There is a 50/50 chance that the donor will be randomized to immediate biopsy processing by
frozen section, versus permanent processing that yields results after transplant. If for any
reason their surgeon feels that it would not be safe to proceed without the biopsy result, he
or she will have the ability to receive the results of the biopsy before the transplant. The
study team will record any episodes of this occurrence.

Inclusion Criteria:

- Kidney transplant candidate

- On waitlist for kidney transplant at the time of informed consent at one of the
participating sites

- Age 18 or older

- Willing and able to provide informed consent for participation in the study

Exclusion Criteria:

- Unable or unwilling to provide informed consent to participate in the study

- Younger than 18 years old

- Not on waitlist for kidney transplant at the time of informed consent at one of the
participating centers

- Candidates for or recipients of multi-organ transplants (kidney along with another
solid organ)
We found this trial at
2
sites
Saint Louis, Missouri 63110
Principal Investigator: Krista Lentine, MD, PhD
Phone: 314-577-8461
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