Pilot Randomized Trial to Define the Benefits and Harms of Deceased Donor Kidney Procurement Biopsies
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 12
- 试验地点
- 2
- 主要终点
- risk-adjusted kidney yield
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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
排除标准
- •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)
研究组 & 干预措施
Procurement Biopsy: Frozen section
In the routine care condition, biopsies will be processed immediately as a frozen section.
干预措施: Procurement Biopsy: Frozen section (Diagnostic Test)
Procurement Biopsy: Permanent section
In the intervention group, the biopsy processing will be delayed to permanent section, and therefore not available until allocation is complete.
干预措施: Procurement Biopsy: Permanent section (Diagnostic Test)
结局指标
主要结局
risk-adjusted kidney yield
时间窗: 3 years
per kidney donor with an immediate vs delayed procurement biopsy processing (this will serve as the primary organ utilization metric, and is the adjusted converse of organ discard)
次要结局
- Number of participants with graft survival(3 years)
- Cold ischemia time(3 years)
- Number of participants with delayed graft function(3 years)
- Life years for transplant recipients(3 years)
- Patient survival after transplant(3 years)
研究者
Krista Lentine MD, PhD
Professor
St. Louis University
